Du Buisson, Kramer, Swart, Bouwer Inc ta Ampath and Others v Health Funders Association Npc and Others (CRP102Oct23/EXC187Dec23) [2025] ZACT 24 (19 February 2025)

78 Reportability
Competition Law

Brief Summary

Competition Law — Excessive Pricing — Self-referral by Health Funders Association and medical schemes alleging excessive pricing by Pathologists for PCR tests during COVID-19 pandemic — Complainants sought declaratory order of contravention of section 8(1)(a) of the Competition Act — Pathologists had previously entered into consent agreements with the Competition Commission regarding similar conduct — Issue of whether self-referral was precluded by section 67(2) of the Act due to completed proceedings — Tribunal dismissed exceptions raised by Pathologists, affirming that the self-referral was valid and did not contravene the Act.

Comprehensive Summary

Summary of Judgment


1. Introduction


The proceedings were exception applications brought before the Competition Tribunal of South Africa in a set of consolidated matters. The exceptions were raised by three pathology groups, namely Drs Du Buisson, Kramer, Swart, Bouwer Inc t/a Ampath (Ampath), Drs Dietrich Voigt, Mia and Partners t/a Pathcare (Pathcare), and Dr Mauff AC and Partners t/a Lancet Laboratories (Lancet) (collectively referred to in the reasons as the Pathologists). The exceptions were directed at a self-referred complaint referral instituted by The Health Funders Association NPC (HFA) and 36 medical schemes listed in an annexure (collectively referred to as the Complainants). The Competition Commission was cited as a respondent in the complaint referral.


The procedural history, as relied upon by the Tribunal, began with a complaint lodged with the Competition Commission by the Council for Medical Schemes (CMS) in October 2021 regarding alleged excessive pricing for COVID-19 PCR tests. The Commission investigated and concluded, on a prima facie basis, that excessive pricing had occurred. This resulted in consent agreements between the Commission and the Pathologists, concluded without admissions of liability, and confirmed as orders of the Tribunal in December 2021.


In March 2023, the Complainants lodged a further complaint with the Commission under the Competition Act. The Commission issued a notice of non-referral in September 2023, reasoning that the Complainants’ complaint was materially similar to the CMS complaint and had effectively been settled through the earlier consent orders. The Complainants then proceeded by way of a self-referral to the Tribunal in October 2023, focusing on alleged excessive pricing for PCR tests during the period March 2020 to December 2021.


The general subject-matter of the dispute concerned whether the Complainants’ referral affidavit properly pleaded a cause of action for excessive pricing under section 8(1)(a) of the Competition Act, including whether it complied with the Tribunal’s pleading requirements. Although the Complainants initially sought relief relating to both section 8(1)(a) and section 4(1)(b), and also sought administrative penalties, those parts were abandoned and the matter before the Tribunal was confined to the sufficiency of the pleadings in respect of the excessive pricing claim and related allegations.


A further contextual feature, addressed by the Tribunal as a preliminary question, was that the Complainants sought a declaratory finding of a prohibited practice to enable civil damages litigation, because section 65(6)(b) requires certification by the Tribunal or the Competition Appeal Court that the conduct has been found to be a prohibited practice.


2. Material Facts


The Tribunal relied on the following material background facts relating to the COVID-19 pandemic and the PCR testing market conditions. COVID-19 emerged internationally in late 2019 and was declared a pandemic by the World Health Organisation on 11 March 2020. South Africa declared a National State of Disaster on 15 March 2020 and implemented a nationwide lockdown beginning 26 March 2020. The Tribunal accepted that these conditions materially disrupted market functioning and contributed to sudden demand spikes for goods and services relevant to healthcare.


The Tribunal accepted as material that PCR tests were regarded as the most accurate and reliable test available to detect COVID-19 during the relevant time, and that demand for PCR testing surged rapidly, contributing to supply constraints. The Tribunal also noted that government issued Consumer and Customer Protection and National Disaster Management Regulations and Directions on 19 March 2020, aimed at addressing exploitation of pandemic conditions, including forms of excessive pricing during the national disaster.


As to the prior enforcement history, the Tribunal accepted that CMS complained to the Commission in October 2021 alleging excessive pricing for PCR tests, premised on laboratories (including the Pathologists) charging R850 (including VAT) per PCR test during the period March 2020 to December 2021. The Commission investigated and concluded, on a prima facie basis, that excessive pricing in contravention of the Act had occurred. On 8 December 2021 the Commission requested price reductions to no more than R500 (inclusive of VAT), failing which it would approach the Tribunal urgently. The Pathologists agreed to the reduction and entered into consent agreements, confirmed as Tribunal orders, without admissions of liability.


Regarding the present referral, the Tribunal accepted that in March 2023 the Complainants lodged a complaint with the Commission alleging contraventions of section 8(1)(a) (excessive pricing) and section 4(1)(b) (an agreement not to reduce prices). The Commission issued a non-referral in September 2023, explaining that the complaint was materially similar to the CMS complaint and had been settled through the earlier consent agreements.


The Tribunal accepted that the Complainants self-referred in October 2023, alleging that the Pathologists charged an excessive price for PCR tests during March 2020 to December 2021, and that the Complainants intended to pursue damages claims in the High Court. The Tribunal treated as material the Complainants’ explanation that they required a finding of prohibited conduct for purposes of section 65(6)(b).


In relation to the exceptions, the Tribunal treated as material the content of the Complainants’ pleaded case that the relevant product market was the market for the supply of SARS-CoV-2 PCR tests (understood by the Tribunal to be PCR testing services), and that the geographic market was pleaded as local due to pandemic conditions affecting movement and consumer choice. The Tribunal also treated as material that the Complainants’ dominance case was pleaded primarily as one of market power (rather than reliance on market share thresholds), and that the Complainants sought to rely on the fact that prices remained high while input costs allegedly decreased, as well as reliance on the reduction to R500 in the consent outcomes as part of their excessive pricing narrative.


The Tribunal distinguished one pleaded aspect as insufficiently particularised at the exception stage, namely the allegation that smaller comparator firms charged substantially lower prices than the Pathologists. The Tribunal considered that the Complainants did not identify the comparator firms, their prices, the relevant markets, or the relevant periods, and that this lack of particularity prevented the Pathologists from answering that part of the case.


3. Legal Issues


The central legal questions were concerned primarily with pleading sufficiency and procedural fairness in the context of exceptions, rather than the final merits of excessive pricing. The Tribunal was required to determine whether, on the pleadings as they stood, the Complainants’ referral affidavit was excipiable on the bases advanced by the Pathologists, including whether it was vague and embarrassing or failed to disclose a cause of action.


A significant preliminary legal question, raised by the Tribunal and addressed by the parties, was whether the Complainants’ self-referral was precluded by section 67(2) of the Competition Act, which bars referral against a firm that has been a respondent in completed proceedings relating substantially to the same conduct. This issue involved interpretation of statutory language (“completed proceedings”) and its interaction with consent orders concluded without admissions of liability, as well as the effect of section 49D(4) (providing that a consent order does not preclude certain declaratory or civil damages relief).


The exceptions required the Tribunal to decide issues that were predominantly questions of law and pleading adequacy, and the application of legal standards to pleaded facts, including whether material facts were sufficiently particularised under Tribunal Rule 15. The Tribunal repeatedly emphasised that the merits would require oral evidence and would not be decided on the papers at the exception stage.


4. Court’s Reasoning


The Tribunal began by setting out its approach to exceptions. Although the Tribunal Rules do not expressly provide for exceptions, the Tribunal relied on Rule 55(1)(b) to have regard to the Uniform Rules of the High Court in procedural gaps. It confirmed that it has previously entertained exceptions and that its approach broadly mirrors that of the High Court, while recognising that Tribunal complaint proceedings are sui generis, often involving complex intersections of law and economics, and that the Tribunal has inquisitorial powers.


In framing the exception test, the Tribunal emphasised fairness and the pleading requirements under Rule 15, namely that the referral must particularise the material facts and the basis for the legal conclusions contended for, so that a respondent can understand the case it must meet. At the same time, the Tribunal stressed that fairness does not compel complainants to provide more at pleadings stage than the Tribunal Rules require, and that exceptions should not become an over-technical scrutiny for minor imperfections.


Before addressing the pleaded grounds, the Tribunal dealt with whether the Complainants’ referral was barred by section 67(2) due to the earlier consent orders arising from the CMS complaint. The Tribunal considered competing submissions about whether consent orders bring “completed proceedings” and about the purpose of section 67(2) in preventing double jeopardy and repeat harassment. The Tribunal referred to authority addressing completion of proceedings and to Tribunal decisions and commentary suggesting that settlements without admissions of liability may terminate proceedings without necessarily precluding later processes aimed at obtaining a prohibited practice finding.


The Tribunal placed weight on section 49D(4), which expressly states that a consent order does not preclude a complainant from applying for a declaration under section 58(1)(a)(v) or (vi), or an award of civil damages under section 65 unless damages are awarded in the consent order. The Tribunal also reasoned that the consent orders appeared forward-looking, did not impose penalties, and did not compensate for past conduct. On that basis, enabling a damages claim for past harm was not treated as raising the double jeopardy concerns that section 67(2) is directed at. The Tribunal further considered the constitutional right of access to courts under section 34 of the Constitution, and concluded that the Complainants’ right to pursue damages (subject to statutory certification requirements) was not extinguished by consent orders without admissions of liability. Accordingly, the Tribunal concluded that the consent orders did not preclude the Complainants from seeking declaratory relief as a necessary step toward civil damages claims.


Turning to the exceptions themselves, the Tribunal grouped the grounds and addressed them in turn.


On market definition, the Tribunal held that the Complainants had pleaded the product market as PCR testing and that, on a favourable reading of the papers, there could be no genuine misunderstanding that the case concerned PCR testing services rather than merely the sale of test kits. The Tribunal noted that at least one Pathologist’s own submissions reflected an understanding of the pleaded market. Regarding the geographic market, the Tribunal accepted that in crisis conditions markets can be narrowly defined due to restrictions on movement, referring to its prior approach in Dis-Chem. It held that the Complainants had set out enough to allow the matter to proceed, with the correctness of market definition to be tested at trial.


On the alleged failure to plead market shares, the Tribunal treated dominance as capable of proof either through market share presumptions or through market power, and accepted that section 7(c) permits dominance to be shown even where market share is below 35% if market power exists. The Tribunal held that the Complainants explicitly relied on market power and pleaded facts said to support that inference, and that the Pathologists were adequately informed that no market share presumption was being invoked and that the onus would rest on the Complainants. Relying on its approach in Babelegi and Dis-Chem, the Tribunal held that market share analysis is not the only tool for assessing market power, particularly in crisis settings. This ground was dismissed.


On the alleged conflation between market power and excessive pricing, the Tribunal rejected the contention that relying on high prices as evidence of both market power and excessiveness was impermissibly circular. It accepted that the Tribunal itself had previously recognised an inferential approach in which the same facts (such as price increases) may support inferences relevant to both dominance/market power and the existence of excessive pricing, referencing its own reasoning in Dis-Chem and the approach endorsed in Babelegi. This ground was dismissed.


On the asserted vagueness as to collective dominance versus individual dominance, the Tribunal held that the referral was clear that the case pleaded was one of individual dominance, including explicit allegations that each Pathologist had market power. It accepted that multiple firms may simultaneously be dominant on pleaded facts, and rejected the suggestion that the referral necessarily relied on collective dominance. This ground was dismissed.


On the alleged lack of clarity regarding the complaint period, the Tribunal found the period was clearly pleaded as March 2020 to December 2021, consistent with the earlier CMS complaint and the consent outcomes. The Tribunal held that whether the evidence ultimately supports the period (or only part of it) was for trial. This ground was dismissed.


On reliance on the COVID-19 Regulations, the Tribunal considered the Pathologists’ argument that the Regulations addressed price increases not linked to costs, whereas the Complainants alleged failure to decrease prices despite cost decreases, and that PCR services did not have a pre-COVID baseline. The Tribunal held that it was arguable that the Regulations could be relevant either through a purposive interpretive approach or as reflecting policy considerations relevant under section 8(3). It held that the Complainants’ pleading sufficiently raised the relevance of the Regulations, and noted its earlier approach in Tsutsumani where the Regulations were applied even in circumstances where a firm had not previously supplied the product. This ground was dismissed.


On whether the Complainants failed to plead facts showing the price was excessive, the Tribunal accepted that the Commission’s earlier conclusions were not binding and were provisional, but nevertheless treated the agreed reduction to R500 as a significant pleaded fact. While acknowledging the theoretical possibility that firms could agree to supply below cost, the Tribunal considered that this was, on its face, improbable, and sufficient at exception stage to support an arguable case that the earlier higher price (R850 or R710 as referenced) could be excessive if R500 was profitable. The Tribunal held that the pleadings were sufficient to proceed, with evidentiary disputes to be resolved at trial. This ground was dismissed.


In dealing with the section 8(3) factors, the Tribunal separated different aspects. It held that the allegation about comparator firms charging lower prices was pleaded in a conclusory manner without identification of the comparator firms, their prices, relevant markets, or time periods. The Tribunal held that the Pathologists could not reasonably be expected to answer that allegation without such particulars, and upheld the exception on that narrow ground, requiring supplementation.


By contrast, on the Complainants’ reliance on the Health Market Inquiry findings, the Tribunal regarded the objection as more akin to disputing the relevance and probative value of evidence rather than revealing a fatal pleading defect, and held that this could be addressed at trial. On the “lucky monopolist” characterisation and related market power theory in crisis conditions, the Tribunal held that the Complainants had pleaded sufficient material facts for the Pathologists to answer, and that the sustainability of the theory would be determined after oral evidence. These grounds were dismissed.


Finally, on detriment, the Tribunal accepted that the Complainants’ case was that excessive pricing of an essential service during a pandemic is inherently detrimental to those who received and paid for it, directly or indirectly. It relied on the approach in Babelegi regarding detriment in crisis circumstances. It held that the Complainants had sufficiently pleaded the factual basis for alleged detriment (including increased scheme claims costs and reserve impacts), and that the extent of harm and any claimed effects on testing volume and virus spread were matters for trial. This ground was dismissed.


5. Outcome and Relief


The Tribunal dismissed the exception applications in almost all respects, and upheld only the exception relating to the Complainants’ insufficiently particularised allegations concerning comparator firms charging lower prices.


The Tribunal ordered the Complainants to deliver a supplementary founding affidavit within 15 business days, identifying the comparator firms by name, their prices, the markets in which they allegedly charged lower prices, and the relevant period(s). The Tribunal then directed Lancet and Pathcare to file answering affidavits within 20 business days of receiving the supplementary affidavit, and directed Ampath to file a supplementary answering affidavit within the same time period. The Complainants were permitted to file a replying affidavit within 10 business days thereafter if they wished.


No costs order was made.


Cases Cited


Competition Commission v Beefcor Proprietary Limited and Another [2003] ZACAC 5; [2003] 2 CPLR 272 (CAC)


Competition Commission v Beefcor Proprietary Limited and Another 2021 (4) SA 408 (CC)


South African Airways v Nationwide and Comair 83/CR/Oct04


Competition Commission South Africa v Sasol Chemical Industries Ltd, In re: Competition Commission South Africa v Sasol Chemical Industries Ltd and Others 45/CR/May06, 31/CR/May05 [2010] ZACT 48; [2010] 2 CPLR 231 (CT) (20 July 2010)


SAPPI Fine Paper (Pty) Ltd v Competition Commission [2003] ZACAC 5; [2003] 2 CPLR 272 (CAC)


Invensys PLC and 2 others v Protea Automation Solutions (Pty) Ltd [1999-200] CPLR 299


Competition Commission of South Africa v Bank of America Merrill Lynch International Designated Activity Company and Others CR212Feb17 [2023] ZACT 26


Competition Commission et al v United South African Pharmacies et al (USAP) [2003] ZACT 4


National Association of Pharmaceutical Wholesalers and Others v Glaxo Wellcome and Other, Case No: 45/CRJul01


Rooibos Ltd v Competition Commission, Case No 129/CR/Dec08


Casalinga Investments CC t/a Waste Rite v The Competition Commission (CR133Sep15/EXC152Oct15)


Competition Commission of South Africa v Dis-Chem Pharmacies Ltd, CR008Apr20


Competition Commission of South Africa v Babelegi Workwear and Industrial Supplies CC [2020] 1 CPLR 152 (CT)


Babelegi Workwear and Industrial Supplies CC v Competition Commission of South Africa 2021 (6) SA 446


Competition Commission v Tsutsumani Business Enterprise CC COVCR113Sep20


Mittal Steel South Africa Limited and Others v Harmony Gold Mining Company Limited and Another [2009] ZACAC 1


Sasol Chemical Industries Limited v Competition Commission (131/CAC/Jun14) [2015]


FFS Refiners (Pty) Ltd v Eskom & Others, Case no 64/CR/Sep02 (decision of 21 February 2003)


Legislation Cited


Competition Act 89 of 1998, sections 4(1)(b), 7, 8(1)(a), 8(3), 49B(2)(b), 49D(4), 51(1), 58(1)(a)(v), 65(6)(b), 67(2), 78


Constitution of the Republic of South Africa, 1996, section 34


Rules of Court Cited


Competition Tribunal Rules, Rule 15 and Rule 15(2)


Competition Tribunal Rules, Rule 55(1)(b)


Uniform Rules of the High Court (referred to as a comparative source under Rule 55(1)(b))


Held


The Tribunal held that the Complainants’ self-referral was not precluded by the prior consent orders concluded between the Commission and the Pathologists, where those consent orders were concluded without admissions of liability and were not treated as extinguishing the Complainants’ ability to seek declaratory relief necessary for later damages litigation. The Tribunal held that the referral affidavit, read favourably and with due regard to the Tribunal’s pleading standards, sufficiently pleaded the material facts necessary for the Pathologists to understand and answer most aspects of the excessive pricing case, with disputed economic and factual issues to be determined at trial after oral evidence.


The Tribunal held, however, that the Complainants’ reliance on comparator firms allegedly charging lower prices was pleaded in a conclusory manner lacking necessary particulars. The Tribunal upheld the exception on that narrow issue and directed the filing of a supplementary affidavit identifying the comparator firms, their prices, the relevant markets, and time periods.


LEGAL PRINCIPLES


The Tribunal applied the principle that, although its Rules do not expressly provide for exceptions, it may entertain exceptions by having regard to High Court procedure under Rule 55(1)(b), while recognising that Tribunal complaint proceedings are sui generis, often involving complex economic analysis, and are conducted with an emphasis on fairness and informality.


In assessing exceptions, the Tribunal applied the principle that the test is whether, on all possible readings of the pleading (interpreted in the manner most favourable to the non-excipient), no cause of action can be made out. The Tribunal emphasised that it must accept pleaded factual allegations as true for purposes of exception, avoid over-technical approaches, and uphold vagueness-and-embarrassment objections only where they go to the root of the cause of action.


The Tribunal applied the pleading standard in Tribunal Rule 15 that the initiating affidavit must particularise the material facts and grounds relied upon so that the respondent can understand the case to meet. The Tribunal emphasised that this fairness requirement does not require a complainant to plead evidentiary detail beyond what the Tribunal Rules demand at the referral stage.


On dominance, the Tribunal applied the principle that dominance may be established either through market share thresholds or by proof of market power, and that market share is not necessarily a jurisdictional pleading requirement where the complainant relies on section 7(c) and pleads market power.


In the context of crisis conditions, the Tribunal applied the approach that market power may be inferred from pricing conduct and surrounding conditions, and that traditional market share and market definition tools, while commonly used, are not the only means of assessing market power in exceptional market circumstances.


On the interaction between consent orders and subsequent relief, the Tribunal applied section 49D(4) as recognising that a consent order does not preclude an application for declaratory relief for purposes of section 65, and reasoned that consent orders concluded without admissions of liability and without penalties or compensation for past conduct do not necessarily preclude later steps aimed at obtaining a prohibited practice finding to enable civil damages claims.

1
COMPETITION TRIBUNAL OF SOUTH AFRICA
In the consolidated exceptions between:1
DRS DU BUISSON, KRAMER, SWART, BOUWER INC
T/A AMPATH
DRS DIETRICH VOIGT, MIA AND PARTNERS
T/A PATHCARE
DR MAUFF AC AND PARTNERS T/A LANCET
LABORATORIES
1stst Applicant
2ndnd Applicant
3rdrd Applicant
And
THE HEALTH FUNDERS ASSOCIATION NPC
THE MEDICAL SCHEMES LISTED IN ANNEXURE “A”
In re the Complaint referral between:2
THE HEALTH FUNDERS ASSOCIATION NPC
THE MEDICAL SCHEMES LISTED IN ANNEXURE “A”
1stst Respondent
2ndnd – 37th
th Respondent
1stst Applicant
2ndnd – 37th
th Applicants
1Case Nos: CRP102OCT23/EXC87DEC23; CRP102OCT23/EXC143DEC23; CRP102OCT23/EXC177FEB24
2CRP102OCT23

2
And
DRS DU BUISSON, KRAMER, SWART, BOUWER INC
T/A AMPATH
DRS DIETRICH VOIGT, MIA AND PARTNERS
T/A PATHCARE
DR MAUFF AC AND PARTNERS T/A LANCET
LABORATORIES
THE COMPETITION COMMISSION
1stst Respondent
2ndnd Respondent
3rdrd Respondent
4thth Respondent
ORDER AND REASONS FOR DECISION
____________________________________________________________________________
INTRODUCTION
[1] This matter concerns three exceptions. They arise from a self-referral by the Health
Funders Association NPC (HFA) and 36 medical schemes listed in Annexure “A” of
the notice of motion (“the medical schemes”).3 The respondents in the self-referred
complaint are the excipients in these matters. They are Dr Du Buisson, Kramer, Swart,
Bouwer Inc t/a Ampath (“Ampath”), Drs Dietrich Voigt, Mia and partners t/a Pathcare
3 They are: Remedi Medical Aid Scheme, SA Breweries Medical Aid Society, Discovery Health Medical
Scheme, Anglo Medical Scheme, TFG Medical Aid Scheme, Malcom Medical Aid Scheme, Bankmed,
LA Health Medical Scheme, Multichoice Medical Aid Scheme, Tsogo Sun Group Medical Scheme,
Momentum Medical Scheme, Glencore Medical Scheme, Massmart Health Plan, Profmed, De Beers
Benefit Society, Sasolmed, Bonitas Medical Fund, Parmed Medical Aid Scheme, AECI Medical Aid
Society, Barloworld Medical Scheme, MBMED Medical Aid Fund, Fedhealth Medical Scheme,
Medshield Medical Scheme, SABC Medical Scheme, SAPS Medical Scheme, SA Municipal union
National Medical Scheme, Retail Medical Scheme, Engen Medical Benefit Fund, Netcare Medical
Scheme, Lonmin Medical Scheme, BMW Medical Aid Society, Wooltru Healthcare Fund, Transmed
Medical Fund.
Panel : G Budlender (Presiding Member)
: M Mazwai (Tribunal Member)
: I Valodia (Tribunal Member)
Heard on : 27 November 2024
Order issued on: 19 February 2025
Reasons issued on: 19 February 2025

3
(“Pathcare”), and Dr Mauff AC and Partners t/a Lancet Laboratories (“Lancet”) –
collectively “the Pathologists”.
[2] The HFA and the medical schemes (“the Complainants”) submitted a complaint to the
Competition Commission (“Commission”) in terms of section 49B(2)(b) of the
Competition Act 89 of 1998 (“the Act"). Following investigation, the Commission
issued a notice of non-referral, and the Complainants then made a self-referral in terms
of section 51(1) of the Act. The self-referral relates to an allegedly excessive price
charged by the Pathologists for PCR tests for the period March 2020 to December
2021.
[3] The Complainants initially sought orders:
3.1 declaring that the Pathologists had each contravened section 8(1)(a) of the Act
for the period March 2020 to December 2021, and had contravened section
4(1)(b) of the Act;
3.2 that the Pathologists are each liable to pay an administrative penalty equal to
10% of their respective annual turnover;
[4] The Complainants abandoned the prayers for orders that the Pathologists have
contravened section 4(1)(b) of the Act, and for orders for payment of an administrative
penalty. There was no opposition to those amendments, which we granted.
[5] Ampath filed an answering affidavit and noted an exception. Pathcare and Lancet both
noted exceptions, but did not file answers. The exceptions deal with similar matters,
and were heard together.
[6] We decided to dismiss the exception applications, except for the exception in relation
to section 8(3) factors: “comparator firms charging lower prices than the pathologists”.
”.

4
[7] These are the reasons for our decision.
THE FACTUAL BACKGROUND
COVID- 19
[8] The first cases of COVID-19 were identified in Wuhan, China in December 2019. By
mid-January 2020, COVID-19 had started to spread beyond the borders of China. On
30 January 2020, the World Health Organisation (“WHO”) declared the COVID-19
outbreak a Public Health Emergency of International Concern.
[9] During January and early February 2020, it was reported that COVID-19 had broken
out in Europe. By then, several countries had imposed restrictions on travel, and
eventually imposed export bans on essential medical and protective supplies. South
Africa reported its first case of COVID-19 on 5 March 2020.
[10] On 11 March 2020, the WHO declared COVID-19 a pandemic for which there is no
cure. On 15 March 2020, the South African government declared a National State of
Disaster. That was followed, on 23 March 2020, by the announcement by the President
that South Africa would be placed under a nationwide lockdown.
[11] The lockdown took effect at 23:59 on 26 March 2020 and was to remain in place,
initially, for 21 days. That 21-day period was just the beginning; lockdowns (or some
other form of COVID-related restrictions) remained in place for approximately two
years. The consequences of the pandemic and the government measures to deal with
it were far-reaching. The normal functioning of markets was seriously disrupted. Of
relevance to this matter, there were sudden spikes in demand for a range of goods,
including personal protective equipment and medical supplies.
[12] Appreciating the risks of the imbalance between supply and demand, and the unequal
bargaining power created by it, on 19 March 2020 Government issued the Consumer

5
and Customer Protection and National Disaster Management Regulations and
Directions. The COVID Regulations were aimed specifically at firms seeking to exploit
the pandemic conditions for economic gain.
[13] A key element in the fight against the spread of the virus was the detection of who was
infected. The single most accurate and reliable available form of testing was the
polymerase chain reaction test (often called the PCR test).
[14] The reliability and accuracy of PCR testing, and the general sense of panic surrounding
COVID-19 and its rampant spread, resulted in a rapid surge of demand for PCR
testing. There was a shortage of supply to meet this demand.
The Complaint by the Council for Medical Schemes
[15] On 8 October 2021, the Council for Medical Schemes (“CMS”) filed a complaint with
the Commission under section 49B(2)(b) of the Act, alleging that certain laboratories
(including the Pathologists) were engaging in excessive pricing in the market for the
supply of PCR tests.
[16] The complaint was premised on the Pathologists having charged a price of R850
(including VAT) per PCR test for the period March 2020 to December 2021.
[17] The Commission investigated the complaint. It concluded, on a prima facie basis, that
the Pathologists were indeed guilty of excessive pricing in contravention of section
8(1)(a) of the Act.
[18] On 08 December 2021, the Commission wrote to the Pathologists and requested that
they agree to reduce their prices to no more than R500 (inclusive of VAT), failing which
the Commission would approach the Tribunal, on an urgent basis, for appropriate
relief. The Pathologists agreed to the Commission's request, and consent agreements
were concluded between the Commission and the Pathologists; and without an

6
admission of liability. Those consent agreements were duly confirmed by, and made
orders of, the Tribunal.4
The complaint
[19] On 2 March 2023, the Complainants submitted a complaint to the Commission, under
section 49B(2)(b) of the Act.
[20] According to the complaint:
20.1 the Pathologists contravened section 8(1)(a) of the Act by having engaged in
excessive pricing in the market for the sale of PCR tests; and
20.2 the Pathologists contravened section 4(1)(b) by reaching an agreement,
arrangement or understanding that they would not reduce their respective
prices for PCR tests.
[21] On 6 September 2023, the Commission issued a notice of non-referral accompanied
by a letter explaining its decision to non-refer. The Commission stated that the
Complainants’ complaint was similar in every material respect to the CMS complaint,
that the CMS complaint had resulted in the consent agreements concluded with the
Pathologists, and that the complaint between the Commission and the Pathologists
had been settled.
The reason for the Complainants’ self-referral
[22] On 05 October 2023, the Complainants self-referred this matter to the Tribunal.
[23] In the self-referral, the Complainants allege that between March 2020 and December
2021, the Pathologists contravened section 8 of the Act by charging an excessive price
4CC v Lancet Case No: COVCO141Dec21;
CC v Ampath Case No: COVCO140Dec21; CC v
Pathcare Case No: COVCO142Dec21

7
for the sale of polymerase chain reaction (PCR) tests, which are used to detect the
COVID-19 virus.
[24] The Complainants allege that these unlawful prices caused the medical schemes to
suffer harm, and that they intend to pursue damages claims against the Pathologists
in the High Court. In order for them to bring such claim, they are required by section
65(6)(b) of the Act to file with the registrar of the High Court, a notice from the Tribunal
or the Competition Appeal Court (CAC) “certifying that the conduct constituting the
basis for action has been found to be a prohibited practice in terms of the Act.”
[25] The Complainants thus brought this referral to obtain from the Tribunal a declaratory
order that the Pathologists are guilty of a prohibited practice. If such a finding is made,
the Complainants will use that finding in claims for damages in the High Court.
COMPLETED PROCEEDINGS
[26] As noted above, the Complainants made this self-referral in the wake of a non-referral
by the Commission on the ground that a complaint concerning the same conduct and
covering the same period had been resolved by the consent orders confirmed by the
Tribunal in December 2021. None of the Pathologists admitted, in the Consent
Agreements, that they had charged excessive prices for COVID-19 PCR tests in
contravention of the Act.
[27] In its non-referral letter, the Commission stated that it was of the view that the “full and
final settlement” clause in the consent agreements has the result that the Commission
cannot pursue any further action against the Pathologists on the facts contained in the
CMS complaint or a complaint relating to the same or similar conduct.
[28] We requested the parties to address us as on whether these applications by the
Complainants are precluded by section 67 of the Act. Section 67(2) provides:

8
“A complaint may not be referred to the Competition Tribunal against any firm
that has been a respondent in completed proceedings before the Tribunal
under the same or another section of this Act relating substantially to the same
conduct.”.”
[29] Ampath had raised this issue in its answering affidavit as a point in limine. At the
hearing, Ampath submitted that the purpose of section 67(2) of the Act is to protect
firms against double jeopardy, and from harassment in the form of repeat referrals
arising out of one and the same conduct. Ampath submitted that for proceedings to be
completed, there must be an element of finality. According to Ampath, the inclusion of
full and final settlement on the consent order brought finality to the CMS complaint,
which covered the same conduct and the same time period as the complaint of the
Complainants, by way of an order of the Tribunal.
[30] Counsel for Ampath drew attention to the judgment of the CAC in Competition
Commission v Beefcor Proprietary Limited and Another,5
where the Court held that
“the word 'completed' in its ordinary and natural meaning can be applied to
proceedings which have come to an end in one way or another - whether following a
trial on the merits, a consent order or an abandonment of the proceedings by way of
withdrawal
.”6 7
[31] Counsel for Ampath submitted that this referral is not to be treated as a self-referral in
substance, but rather as an application for a declaratory order as a precursor to a claim
for damages. Counsel submitted that Complainants’ rights are limited: while they
5 [2003] ZACAC 5; [2003] 2 CPLR 272 (CAC)
6 Ibid at para 53.
7 On appeal to the Constitutional Court, the Court limited its finding to the nature and consequences of
a withdrawal. Competition Commission v Beefcor Proprietary Limited and Another 2021 (4) SA 408
(CC).

9
cannot seek remedial relief, they can seek a declaratory order for the purposes of
seeking damages in due course.
[32] Counsel for Pathcare referred to Competition Commission vSouth African Airways v
Nationwide and Comair (Comair),8
where the Tribunal reasoned that upon an
admission of liability by the respondent, the proceedings before the Tribunal are
completed.9
[33] Counsel for Lancet concurred with the submissions made by Ampath and Pathcare. In
addition, it argued that the Tribunal in Competition Commission South Africa v Sasol
Chemical Industries Ltd, In re: Competition Commission South Africa v Sasol Chemical
Industries Ltd and Others (SCI)1010considered whether a complainant’s or any other
person’s rights had been extinguished in terms of section 67(2) by a settlement which
contained no admission of liability. The Tribunal concluded that it did not consider a
settlement agreement that contains no admission of liability as completed proceedings
for section 67(2) of the Act.11
11
[34] Counsel for Lancet quoted from Sutherland & Kemp, as follows:1212
“...to the extent that the respondent does not admit liability in the consent order:
(a)The Tribunal makes no finding or determination that the conduct complained of
amounts to a contravention of the Act;
(b)A complainant may apply to the Tribunal for a declaration that the respondent’s
conduct constitutes a prohibited practice or a declaration that the whole or any
part of an agreement is void, and it may seek damages against the respondent in
a civil court (unless the consent order already contains an award of damages in
8South African Airways v Nationwide and Comair 83/CR/Oct04.
9 Ibid at paras 59-60.
1010 45/CR/May06, 31/CR/May05 [2010] ZACT 48; [2010] 2 CPLR 231 (CT) (20 July 2010).
1111 Ibid at paras 22 -31.
1212Sutherland & Kemp, Competition Law of South Africa 11.6.4.

1010
that complainant’s favour, in which case it waives its right to seek civil
damages).”13
13
[35] Having regard to the above, Lancet submitted that to the extent that liability is not
admitted in the consent agreement, those proceedings are terminated, but not
completed, and a complainant or another person can refer the complaint to the
Commission, relating to substantially the same conduct, in order to be able to seek the
further remedies against the respondent.
[36] The Complainants submitted the effect of section 49D (4) is that irrespective of any
consent orders, the Tribunal is empowered to grant declaratory relief. Section 49D (4)
provides that
"A consent order does not preclude a complainant from applying for —
(a) a declaration in terms of section 58(1)(a)(v) or (vi); or
(b) an award of civil damages in terms of section 65, unless the consent order
includes an award of civil damages to the complainant."
[37] Section 58(1)(a)(v) — which is referred to in section 49D(4)(a) — provides that “ In
addition to its other powers in terms of this Act, the Competition Tribunal may make an
appropriate order in relation to a prohibited practice ... including declaring conduct of
a firm to be a prohibited practice in terms of this Act, for purposes of section 65.”
[38] The Complainants further submitted that the phrase "completed proceedings
" in
section 67(2) does not immunise a respondent from all repeat referrals. Furthermore,
the protection afforded by section 67(2) only applies where the Tribunal has decided
the merits of the complaint, or the respondents have admitted liability.
1313 Sutherland & Kemp, Competition Law of South Africa 11.6.4.

1111
[39] In SAPPI Fine Paper (Pty) Ltd v Competition Commission14
14the Court held that the
purpose of section 67(2) is to protect firms against double jeopardy.1515 The Court
further held that there are two primary jurisdictional facts or requirements to be satisfied
for the operation of the section. These are (i) the complaint must relate to substantially
the same conduct, and (ii) in respect of which a firm was a respondent in completed
proceedings.1616
[40] The consent orders do not purport to impose a penalty on the Pathologists, or require
them to compensate for their past conduct. On the papers before us, the consent
orders are forward-looking, relating to the future conduct of the Pathologists. We do
not think enabling the Complainants to claim damages as compensation for past
conduct gives rise to double jeopardy.
[41] The Complainants have a right, under section 34 of the Constitution, to access to
courts in order to have their dispute with regard to a claim for damages determined.
That right is constrained by the requirements of section 65(6)(b). In our view, the right
is however not extinguished by a consent order which contains no admission of liability.
This approach is consistent with the precedent to which we have referred above.
[42] We are therefore of the view that the consent orders concluded between the
Commission and the Pathologists do not preclude the Complainants from applying for
a declaratory order as a necessary element of the process of seeking to establish and
enforce a claim for damages.
[43] The Complainants and the Pathologists were in agreement, at the hearing, that the
determination of the merits of the complaint and whether a declaratory order should
1414 [2003] ZACAC 5; [2003] 2 CPLR 272 (CAC).
1515 Ibid at para 4.
1616 Ibid at para 42.

1212
be made cannot be decided on the papers, and oral evidence will need to be led in
that regard.17
17
[44] We now address the three exceptions.
OUR APPROACH TO EXCEPTIONS
[45] The Competition Tribunal Rules (“Tribunal Rules”) do not expressly provide for
exceptions. Rule 55(1)(b) provides that if a "question arises as to the practice or
procedure to be followed in cases not provided for" by the Tribunal's Rules, the
Tribunal may "have regard
" to the Uniform Rules of the High Court.
[46] The Tribunal has previously heard and decided exceptions pursuant to its powers
under Rule 55(1)(b). The Tribunal’s approach to exceptions largely mirrors that of the
High Court.
[47] In Invensys PLC v Protea Automation Solutions (Pty) Ltd (“Invensys”),
1818the Tribunal
stated that there are three central considerations in its approach to exceptions:
47.1 Complaint proceedings in the Tribunal are sui generis and contain elements of
both motion and trial proceedings of the High Court;19
19
47.2 The subject matter of the Tribunal’s proceedings involves the intersection of
law and economics, often requiring complex economic analysis of the facts to
advance a theory of harm; and 2020
1717 Transcript lines 4-20,p4, Transcript lines 1-4, p5, and Transcript lines 5-18 p7.
1818Invensys PLC and 2 others v Protea Automation Solutions (Pty) Ltd [1999-200] CPLR 299.
1919 Ibid at Para 14.
2020 Ibid at Para 15.

1313
47.3 The Tribunal enjoys inquisitorial powers and is required to exercise these in its
carrying out its functions, while ensuring the proceedings are conducted fairly
and informally.21
21
[48] The Tribunal is guided by the principle of fairness, and the standard for referral set out
in Rule 15 of the Tribunal’s Rules.22
22 In order for a referral to meet the requirements of
Rule 15(2), it must particularise the material facts upon which the complaint is founded,
and upon which the legal conclusions for which it contends are based. Fairness
requires that a respondent must be able to understand the case being made out
against it.2323 Fairness however is not a one-way street, and in particular does not oblige
the Commission and private complainants to make more known of the case at
pleadings stage than is required in the Tribunal Rules.24
24
[49] In Competition Commission of South Africa v Bank of America Merrill Lynch
International Designated Activity Company and Others, the Tribunal held that: 2525
49.1 The test on exception is whether on all possible readings of the pleading no
cause of action may be made out;
49.2 Exceptions must be judged on the interpretation of the pleadings most
favourable to the plaintiffs;
49.3 The onus rests on the excipient;
49.4 A court must take all the allegations at face value. The allegations of fact must
be accepted as true and correct;
2121 Ibid at Para 16.
2222Competition Commission et al v United South African Pharmacies et al (USAP) [2003] ZACT 4 at p
2.
2323USAP at p 2; National Association of Pharmaceutical Wholesalers and Others v Glaxo Wellcome and
Other, Case No: 45/CRJul01 (, National Wholesalers') at p 18, para 55;
Rooibos Ltd v Competition
Commission (Rooibos), Case No 129/CR/Dec08, para 6.
2424 National Wholesalers at p18, at para 55; Rooibos Ltd v Competition Commission, Case No
129/CR/Dec08, paras 7-8.
2525 CR212Feb17 [2023] ZACT 26 paras 52 - 53.

1414
49.5 An over-technical approach must be avoided. The purpose of the exception is
not to scrutinise pleadings for every possible flaw and imperfection; and
49.6 An exception that the pleadings are vague and embarrassing will be upheld
only if it goes to the root of the plaintiffs’ cause of action, and not to a particular
paragraph or allegation;
[50] An exception is not about the granularity of the facts alleged.26
26 The affidavit must
contain sufficient ‘concise statements’ of the grounds relied upon and
’material facts
or point of law’ relied upon.27
27The usual remedy for exception applications brought on
the basis of vague and embarrassing pleadings or a failure to disclose a cause of
action is to grant the offending party an opportunity to amend its pleadings. In certain
circumstances, such as when the exception concerns a pure point of law which might
be determinative of the matter, dismissal of the case might be an appropriate remedy.
THE EXCEPTIONS
[51] The exceptions raised by the three Pathologists deal with similar issues. We have
accordingly decided to group the grounds of exception.
[52] The grounds of exception can be categorised as follows:
52.1 Failure to define the relevant market;
52.2 Failure to plead the respective pathologists’ market shares;
52.3 Failure to distinguish between market power and excessive pricing;
52.4 Failure to make it clear whether this is case of alleged collective dominance or
individual dominance;
52.5 Failure properly to set out the complaint period;
52.6 No cause of action based on the COVID-19 Regulations;
2626 Ibid.
2727 Ibid.

1515
52.7 Failure properly to plead facts demonstrating that the price is excessive;
52.8 Section 8(3) factors:
52.8.1Unsustainable reliance on the findings in health market inquiry;
52.8.2Vague reference to Comparator’s firm’s prices
52.8.3Unclear reliance on the “lucky monopolist” theory; and
52.9 Failure properly to plead detriment
First ground of exception: market definition
Product market definition
[53] The Complainants in their referral submitted that the relevant product market is the
market for the supply of SARS-CoV-2 PCR tests.
[54] Lancet argued that the Complainants have not properly defined the relevant market.
Lancet argued that it appears that the product market contended for is the supply of
the tests themselves and not the design and operation and administration of the tests,
but that the self-referral is inconsistent in this regard. Lancet further argued that the
Complainants identify features of PCR tests to delineate the alleged relevant product
market from a demand perspective and distinguish it from Antibody tests. Lancet
contended that none of the features concern the ancillary services related to the tests
that are offered by pathologists such as Lancet.
[55] Lancet further argued that the utility of the SSNIP test (“the small but significant and
non-transitory increase in price” test) is unclear. According to Lancet, the Complainants
simply state the hypothetical questions that one would ask if the SSNIP test were to
be applied to “the prices of PCR tests”, without doing the analysis or stating what the
outcome of the analysis would be and why. The Complainants do not say whether the
SSNIP test would exclude the Antibody tests and how the SSNIP test applies at

1616
different times during the complaint period, given the allegation that Antibody tests
were only approved on 21 July 2021, nor what the other possible substitute products
are to which the SSNIP test applies.
[56] The Complainants responded that on a balanced reading of the self-referral affidavit,
it is clear that the case is concerned not with the sale of PCR test kits, but rather with
PCR testing. The Complainants submit that this is made clear in several places in the
self-referral affidavit. For instance, in paragraph 25.2 of the self-referral affidavit it is
stated that the Pathologists’ prices had remained unchanged in circumstances where
their input costs (particularly in the form of PCR test kits) decreased between March
2020 and September 2021. It was thus clear that PCR test kits are one of the
pathologists’ input costs, i.e. one component of the testing service.
[57] The Complainants pointed out that paragraph 40 of the self-referral affidavit states that
under pandemic conditions, “consumers are far more likely to choose a service
provider nearer to their home or work.” They contended that it is therefore clear that
the relevant product market concerns the provision of services, as opposed to solely
the sale of test kits.
[58] The Complainants further noted that the Tribunal press release which states that
“Lancet agrees … to reduce the price of COVID-19 PCR tests to no more than R500,
inclusive of VAT.” They contended that Lancet’s settlement agreement shows that it
knows full well that the issue is the price charged for PCR testing, and not for the sale
of PCR test kits.
[59] The Complainants pointed out that the cover letter to the self-referral affidavit stated
that the referral concerns “COVID-19 PCR testing prices
”. This, they asserted, makes
it clear that the focus is on the price charged for the testing service as opposed to the
price charged for on-sale of test kits.

1717
[60] A prerequisite for the dominance tests is defining the relevant market in which the firm
alleged to be dominant operates. The purpose of market definition in abuse of
dominance cases is to assess whether a firm is dominant for the purposes of section
7 of the Act. The question is whether the Complainants have properly defined the
relevant market in its referral. On the papers before us, in our view cannot be any
genuine misunderstanding in this regard. Ampath does not appear to have had any
real difficulty in understanding the product market. Its heads of argument state “Butof
course the market that has been defined is the market for PCR testing”.
”.2828 Pathcare
does not appear to have had any difficulty in understanding what the product market
is. It does not raise this objection.
[61] In our view, applying the well-established tests for determining an exception, this
ground of exception is not well-founded, and it is dismissed.
Geographic market definition:
[62] The Complainants submit that “[‘f]rom a geographic perspective, the market is a narrow
one. That is because under pandemic conditions – including restrictions on movement
and fears of being away from home - consumers are far more likely to choose a service
provider nearer to their home or work.
This means that the geographic market is local.
This accords with the position advanced by Lancet in the Commission's healthcare
inquiry, in which Lancet argued that it competes with other pathology practices in
narrowly defined geographic markets.” 2929
[63] The Pathologists contended that the Complainants have failed properly to define the
relevant geographic market. Lancet noted that the Complainants plead that from a
geographic perspective, the market is a narrow one, and that the geographic market
2828 Ampath’s HOA para 75 at p35 of the consolidated HOA bundle.
2929 Applicants’ self-referral affidavit para 40 at p22 of the hearing bundle.

1818
is local. They contended that this conclusion is premised on the bald allegation that
under pandemic conditions, including restrictions on movement and fears of being
away from home, consumers are far more likely to choose a service provider nearer to
their home or work.
[64] Lancet pointed out that the Complainants, as medical schemes, have access to
information as to where their members reside and work and from where their members
obtained the COVID-19 tests that were paid for by the medical schemes. Yet none of
this information appears to form the basis for the conclusion that the market is both
“narrow” and “local,” nor is it possible to ascertain what either term means.
[65] The Pathologists submit that the Complainants do not allege whether it is the radius
around a service provider or the radius around a person’s home or work that
constitutes the alleged relevant “local” market. They further argued that it is not clear
what is meant by the geographic markets being “narrow” or “local.” They contended
that local may be: (i) a portion of one of the nine provinces; (ii) a municipal area; (iii) a
city; (iv) a town; (v) a suburb in a town or city; (vi) a particular area around a focal point
e.g. a shopping centre or a hospital or a clinic or a laboratory or a testing station; (vii)
some other area; or (viii) combinations of the above.
[66] We note that in Competition Commission v Dis-Chem Pharmacies Limited
(Dis-Chem)30
30, we held that in a crisis such as this, markets are narrowly defined
because of the limitation of consumer movement.31
31 This is of equal application to the
present matter.
[67] After hearing the evidence, the Tribunal will decide whether the Complainants
allegations can be sustained. At this stage, however, the Complainants have
3030Competition Commission of South Africa v Dis-Chem Pharmacies Ltd, CR008Apr20
3131 Ibid at para 175.

1919
sufficiently set out the material facts necessary for the Pathologists to answer to the
allegations.
[68] In the light of the above, this ground of exception in unfounded, and it is dismissed.
Second ground of exception: Failure to plead the respective Pathologists’ market
shares
[69] Only a dominant firm can contravene section 8 of the Act. To be dominant, the firm in
question must fit one or more of the definitions in section 7 of the Act, which stipulates
that a firm is dominant if:
“(a) It has at least 45% of that market
(b)It has at least 35% but less than 45% of that market, unless it can
demonstrate that it does not have market power; or
(c) It has less than 35% of that market but has market power.”
[70] Dominance can be established in two ways – through the firm’s market share or by
demonstrating that the firm has market power.
[71] Ampath stated in its heads of argument that assessing dominance is a combination of
a consideration of a firm’s market share and its market power. It asserted that “… it is
to be expected that the pleader at least alleges the market shares said to be enjoyed
by the firm alleged to be dominant, even if reliance is placed on the presence of market
power to establish dominance”.”
3232 Similarly, Pathcare submits that “[t]he identification
3232 Ampath’s HOA para 28 at p14 of the consolidated HOA bundle.

2020
of market shares … is critical for an assessment of ‘dominance’, including the question
of ‘market power’ …”.3333
[72] Lancet appears to have accepted that pleading market share is unnecessary where
the pleaded case is one of market power, as it made no argument regarding market
share.
[73] The Complainants submitted that these grounds of exception are unsustainable for
several reasons.
[74] The plain wording of section 7 demonstrates that market share was not intended by
the legislature to be a jurisdictional requirement of dominance. Dominance is
established through evidence of high market share “or” market power. The
Complainants submitted that the Pathologists cited no authority for the assertion that
the allegation of market share is a jurisdictional requirement.
[75] Pathcare relied on our decision in FFS Refiners34
34for its submission in this regard.
There, we noted that dominance can be established by alleging that the respondent
firm falls into any of the three categories set out in section 7, or if the Complainant is
uncertain, by alleging more than one as alternatives. The respondent firm needs to
know from the complaint what case it is to meet, whether any presumptions apply, and
where the onus lies.
[76] In their self-referral affidavit, the Complainants pin their colours firmly to an allegation
that the Pathologists had market power. They allege facts which, they assert,
demonstrate that the Pathologists had market power.3535 They contend that these facts
are evidence of the Pathologists’ power to act to an appreciable extent independently
of customers. The Complainants do not rely on any presumption arising from the
3333 Pathcare’s HOA para 4.2 at p105 of the consolidated HOA bundle.
3434 FFS Refiners (Pty) Ltd v Eskom & Others Case no 64/CR/Sep02, decision of 21 February 2003.
3535 Complainants’ self-referral affidavit pars 43-54 at pgs 23-54 of the hearing bundle.

2121
provisions of section 7 of the Act, and the onus will therefore fall squarely on them.
The Pathologists have been informed that this is the case they will have to meet.
[77] The Complainants also submitted that in a crisis it would be irrational to insist on market
share being pleaded, because market share says nothing about market power in a
crisis. They rely on the Tribunal’s decision in Competition Commission of South Africa
v Babelegi Workwear and Industrial Supplies CC
3636 where we found that Babeleg
enjoyed market power even though it had a market share of less than 5%, and it was
accordingly dominant.
[78] Our approach to the application of section 7(c) of the Act is set out in Babelegi and
Dis-Chem.
3737In both of those cases, the market definition and market share analysis
were not undertaken in establishing market power. In Dis-Chem, we accepted that
market share and defining the relevant market are usually the tools used to assess a
firm’s market power. However, these are not the only tools available to a competition
regulator.38
38
[79] In our view, the Complainants sufficiently set out the facts to allege market power as
envisaged in section 7(c) of the Act for the Pathologists to understand the case they
must meet. The hearing of evidence will enable a determination of whether the
Complainants' allegations of dominance through market power can be sustained. We
find that at this stage, the Complainants have sufficiently identified the case which the
Pathologists have to meet.
[80] This ground of exception is therefore without foundation and is dismissed.
3636 [2020] 1 CPLR 152 (CT)
3737 Case No: CR000pr20
3838Dis-Chem at para 102.

2222
Third ground of exception: Failure to distinguish between market power and excessive
pricing
[81] The Pathologists contend that it is not permissible for the Complainants to rely on
allegedly unreasonably high prices or margins as evidence of market power.
[82] Ampath submits that high prices or profits alone are not sufficient to show substantial
market power. It further submitted that in making out a case for market power in a
section 8(1)(a) case, more must be alleged than high prices.
[83] Lancet submitted that placing reliance on the same allegedly unreasonably high prices
as evidence of market power and as evidence of excessive pricing is “circular.” It
contended that it is “logically inconsistent” for unreasonably high prices to serve as a
fact that can be used for determining dominance.
[84] The Complainants relied on the Tribunal’s decision in Dis-Chem and the CAC’s
decision in Babelegi
39
39The Tribunal stated in Dis-Chem: “…
the Commission adopts
an inferential approach to the issue of market power and the same facts that serve to
infer market power namely Dis-Chem’s price increases are also relied upon to
establish the excessiveness of the prices.”4040 The Commission thus approached Dis-
Chem in the same way as the Complainants do here, relying on unreasonably high
prices as evidence of market power and as evidence of the existence of market power
and its abuse.
[85] In Babelegi, the CAC noted at paragraph 30: “…
a fundamental part of appellant’s case
on appeal was based on the argument that the tribunal had failed to distinguish
between market power and excessive pricing…”
4141 The Court found that the pandemic
3939Babelegi Workwear and Industrial Supplies CC v Competition Commission of South Africa 2021 (6)
SA 446
4040Dis-Chem at para 102
4141Babelegi (CAC) at para 30.

2323
had altered market conditions to confer on the appellant market power that allowed it
to act like a monopolist for six weeks, extracting the maximum price it was able to
obtain from anxious customers. Though sourced in unprecedented market conditions,
its ability to price in this manner was reflective of market power.4242
[86] The Complainants contended that both the Tribunal and the CAC found nothing
objectionable in unreasonably high prices or margins serving as evidence of two
distinct questions, market power (for purposes of section 7) and prima facie excessive
pricing (for purposes of section 8). The Complainants further contend that if a firm is
shown to be able to charge utterly exorbitant prices, then it has market power and it is
engaging in excessive pricing.
[87] This ground of exception is without merit, and is dismissed.
Fourth ground of exception: Failure to make it clear whether this is a case of collective
dominance or individual dominance.
[88] The Pathologists contend that the allegation of dominance is impermissibly vague, as
it is not clear whether the Complainants’ case is one of collective dominance or one of
individual dominance.
[89] Lancet notes that the Complainants conclude that, in light of the allegations they make,
“for the period March 2020 to December 2021 the pathologists each had market power
in the market for the supply of PCR tests
.”4343 It was submitted that notwithstanding the
use of the word “each”, the allegations leading up to this conclusion refer to “the
4242 At paras 51-56.
4343 Lancet’s HOA para 41 at p67 of the consolidated HOA bundle (emphasis added); referring to para
54 of the Complainants’ self-referral affidavit at p26 of the hearing bundle.

2424
pathologists”, and this (it was submitted) can only refer to the respondents collectively.
It was submitted that collective dominance is not recognised by South African law.
[90] Counsel for the Complainants submitted that the case pleaded in the self-referral
affidavit makes it plain that this is a case of individual dominance.44
44 For instance, in
paragraph 50 of the self-referral affidavit, the Complainants assert submit that “[t]hat
is a further basis on which each of the pathologists should be found to be dominant.”
And paragraph 54 of its self-referral affidavit explicitly alleges that each of the
Pathologists had market power.
[91] The Complainants submitted that a foundational principle in exceptions is that the
pleading must be afforded its most favourable reading. They submitted that read in its
most favourable light, the case advanced in the referral is one of individual dominance.
[92] Relying on the CAC’s finding in Babelegi, the Complainants contended that there is
nothing objectionable in more than one firm being held to be simultaneously
dominant.45
45
[93] We are required to determine whether the Complainants' pleadings comply with
Tribunal Rule 15. In doing so, we must be guided by the principle of fairness that a
respondent is entitled to understand the case against it and cannot “be expected to
answer to any pleading, regardless of its impoverishment of fact or legal averment.”
4646
We are satisfied that the Complainants' self-referral is clear that the case pleaded is
one of individual dominance and meets this standard.
[94] In our view this ground of exception is not well-founded. It is dismissed.
4444 Transcript line 1-5,p166.
4545 CAC at para 49
4646Casalinga Investments CC t/a Waste Rite v The Competition Commission
(CR133Sep15/EXC152Oct15) ("Casalinga") at para 28. See also Invensys, supra at para 31.

2525
Fifth ground of exception: Failure properly to set out the complaint period
[95] The Complainants in their self-referral affidavit stated that the complaint period is
March 2020 to December 2021. This period appears to have been drawn directly from
the Commission’s finding, as reflected in the Pathcare consent order. that:
“The Commission’s investigation also revealed that the pathology groups have
been earning significant profits since March 2020, especially in the current
financial year to date.”
4747
[96] Ampath contended that when it comes to the period for which the “conduct that forms
the basis of this referral persisted”, there is an absence of material facts pleaded.
48
48
Similarly, Lancet contended that the complaint period is vaguely pleaded, because it
not disclose at what point either at the start of or during this complaint period the
Pathologists’ input costs decreased, and sales volumes increased.
[97] We are not persuaded by the Pathologists' submissions that the complaint period is
unclear. The Complainants have set out in the notice of motion, and in their self-referral
affidavit, that the complaint period is March 2020 to December 2021. This is consistent
with the CMS complaint and the consent agreements concluded with the Commission.
Whether the facts justify reliance on this period, or part of it, will have to be determined
at the trial.
[98] In our view this ground of exception is not well-founded. It is dismissed.
4747 Pathcare Consent agreement Para 4.3 at p63 of the hearing bundle.
4848 Lancet’s HOA para 74 at p35 of the consolidated HOA bundle

2626
Sixth ground of exception: No cause of action based on the COVID-19 Regulations
[99] The Pathologists submitted that the Complainants cannot rely on the Consumer and
Customer Protection and National Disaster Management Regulations and Directions
(regulations).49
49 The regulations are aimed at protecting consumers from inter alia
excessive pricing during the COVID outbreak.
[100] Section 8(3) of the Act provides that:
“…Any person determining whether a price is an excessive price must
determine if that price is higher than a competitive price and whether such
difference is unreasonable, determined by taking into account all relevant
factors, which may include—
……………….
(f) any regulations made by the Minister, in terms of section 78 regarding the
calculation and determination of an excessive price.” (emphasis added)
[101] The regulations were published (a) to promote concerted conduct to prevent an
escalation of the national disaster and to alleviate, contain and minimise the effects of
the national disaster; and (b) to protect consumers and customers from
unconscionable, unfair, unreasonable, unjust, or improper commercial practices during
the national disaster. The regulations apply to inter alia private medical services
relating to the testing of the COVID-19 during the period of the national disaster, with
effect from 19 March 2020. They were in force at the time of the alleged prohibited
practice.
[102] The regulations seek to prevent dominant firms from so-called price gouging by
charging high prices for essential goods and services where those prices do not bear
4949 Govt Notice R350 of 19 March 2020.

2727
any relationship to the costs of providing those goods or services, or represent a
substantial increase in average margin or mark-up for those goods or services. In
Competition Commission v Tsutsumani Business Enterprise CC
5050we held that: "(t)he
relevant economic test for determining whether a price is excessive in the context of
the COVID-19 pandemic, as contemplated in Regulation 4 of the Consumer Protection
Regulations, is whether prices charged have any corresponding cost justification from
the supplier up the value chain.”51
51
[103] The Complainants relied on regulation 4.2, which provided:
“ln terms of section 8(3)(f) of the Competition Act during any period of the national
disaster, a material price increase of a good or service contemplated in Annexure A
which-
4.2.1. does not correspond to or is not equivalent to the increase in the cost of
providing that good or service; or
4.2.2 increases the net margin or mark-up on that good or service above the
average margin or mark- up for that good or service in the three-month period
prior to 1 March 2020,
is a relevant and critical factor for determining whether the price is excessive or unfair
and indicates prima facie that the price is excessive or unfair
."
[104] The Pathologists submitted that the regulations target firms that increase prices with
no underlying cost increase, whereas the complaint against the Pathologists is that
they are said to have priced excessively because they failed to decrease prices when
underlying costs decreased. They further contended that the regulations are in any
5050 COVCR113Sep20.
5151 Ibid at para 46.

2828
event not applicable because the PCR test service did not exist pre-COVID, so there
is not a pre-COVID price with which the post-COVID price can be compared. They
submitted that the reliance in the self-referral affidavit on the regulations was
impermissible.
[105] In response, the Complainants submitted that the Commission’s investigations which
led to the conclusion of the consent agreements found that “failure to reduce prices in
the context reductions in costs is the flip side of the COVID-19 Regulations as it results
in the same effect, namely an increase in the margin earned for an essential product”.
”.5252
Counsel contended in his oral submissions that the regulations must be given a
purposive interpretation which applies their principle to the “flip side” situation which
existed in relation to PCR tests, namely a reduction in input price not leading to a
corresponding reduction in the price at which PCR tests were provided.
[106] It is not necessary to decide, at this stage, whether a purposive interpretation would
have that result. In our view, it is arguable that the regulations may be relevant in one
or both of the following respects:
106.1First, it is arguable that through a purposive interpretation, they are applicable
to a failure to decrease prices;
106.2Second, it is arguable that the policy which underlies the regulations is a
relevant factor in terms of section 8(3) of the Act in determining what is an
“excessive” price.
[107] The self-referral affidavit clearly makes the second of the two arguments above.53
53 In
our opinion, having regard to the approach to interpreting pleadings in the context of
5252 Consent order between Pathcare and CC, para 2.5 at p60 of the hearing bundle.
5353 Self-referral affidavit paras 57-60 pgs 28-30 of the hearing bundle.

2929
an exception, it also opens up the permissibility of the first (interpretive) argument. We
find that the Complainants have sufficiently set out the material facts necessary to raise
the interpretation of the regulations as an issue.
[108] In Tsutsumani, we found the regulations to be applicable even though Tsutsumani had
not previously supplied masks. The reasons for that conclusion are set out fully in that
case.
[109] It follows that this ground of exception is without foundation, and is dismissed.
Seventh ground of exception: Failure to plead facts demonstrating that the price is
excessive
[110] The Pathologists except on the basis that the Complainants have failed properly to
plead facts demonstrating the charging of an excessive price.
[111] The first fact alleged by the Complainants in this regard is that between March 2020
and December 2021 the Pathologists’ input costs decreased significantly, but their
selling prices remained unchanged. It is alleged that this resulted in each of the
pathologists "earning significant profits since March 2020, especially in the current
financial year to date.”
[112] In response, the Pathologists contended that the Complainants have not provided any
evidence of a significant decrease in input costs, and that there is therefore no basis
for that allegation.
[113] The second fact alleged by the Complainants is that the Pathologists were each able
to consistently maintain their prices at R850 in circumstances where R500 was found

3030
to be a profitable selling price. They contended that this mark-up of 70% above what
is already a profitable price is, on its face, exorbitant.
[114] The Pathologists asserted that the Complainants rely on the Tribunal’s press release
of 12 December 2021 and the consent agreement concluded between the Pathologists
and the Commission, and the Commission’s prima facie view that the Pathologists
were capable of profitably selling PCR tests at R500. The Pathologists argue that the
Complainants plead no facts to support the Commission’s conclusion on which they
seek to rely.
[115] Ampath argued that the Consent Order does not set out any facts on which the
Commission relied on for its conclusions. Ampath argued that the Complainants
offered no facts of their own, apart from the allegation that the R850 price was
maintained from March 2020 to December 2021, but that fact is inconsistent with the
press release, which records that Ampath had reduced its price to R710 in November
2021.
[116] Ampath also submitted that the price charged for the PCR test was set through the
regulatory process of the Department of Health, and consistent with its Regulations.
[117] Pathcare argued that the consent order cannot be relied upon as prima facie evidence.
Counsel submitted that the Complainants must provide evidence to establish that the
Pathologists were capable of profitably selling PCR tests at R500. Counsel further
contended that the Complainants cannot rely on the Tribunal’s press release as this
was issued before Pathcare’s consent agreement was signed.
[118] Lancet submitted that the Complainants do not plead a competitive price, and instead
rely on statements which are not material facts contained in the consent agreement
between Pathcare and the Commission. Lancet contended that it is unclear when, it is
alleged, the R500 price became a profitable price. Furthermore, that it is unclear

31

whether it is alleged that the competitive price remained consistent during the
complaint period or changed because of the changes in input costs and volumes (and
if so, when it changed and how).

[119] The Complainants relied heavily on four cases in support of their submissions: Mittal
Steel South Africa Limited and Others v Harmony Gold Mining Company Limited and
Another (Mittal), 54 Sasol Chemical Industries Limited v Competition Commission
(SCI),55 Babelegi and Tsutsumani. In SCI, the CAC found that a 20% mark-up may be
permissible but anything above that would raise concerns.56 In Babelegi and
Tsutsunami, we found that where there is evidence of a firm substantially increasing
its prices without any corresponding rise in costs, that constitutes prima facie evidence
of excessive pricing.

[120] The Complainants contended that it is for the respondent firms to adduce evidence to
the contrary if it is to avoid the case against it becoming conclusive.

[121] The conclusions reached by the Commission are not binding on us. They are
provisional, and we do not know on what legal and factual bases they were arrived at.
While they should not be ignored, they cannot be of more than persuasive value.
However, the fact remains that the Pathologists agreed to reduce their price to R500.
While it is hypothetically possible that they agreed to sell the tests below cost , that is
on its face improbable. That probability arises from the agreed facts. It can be rebutted
by evidence, but it is sufficient at exception stage. If the price of R500 per test was
profitable, it is arguable that the earlier price of R850 (or R710) was excessive. We
conclude that at this stage of the pleadings, the Complainants have sufficiently set out
material facts necessary to demonstrate that the price is excessive. Whether that

54 [2009] ZACAC 1
55 (131/CAC/Jun14) [2015]
56 SCI supra at para 175.

3232
conclusion will be found to be justified on all of the facts, is for the Tribunal to decide
after hearing the evidence.
[122] This ground of exception is therefore not justified, and it is dismissed.
Eighth ground of exception: Section 8(3) factors
[123] The Complainants pleaded a number of the section 8(3) factors, including that smaller
firms were charging substantially less than the Pathologists, that markets of this nature
are characterised by high barriers to entry, and that the pandemic conditions had
conferred upon the Pathologists a position of unusual economic strength vis-a-vis their
customers.
[124] Section 8(3) of the Act states:
“Any person determining whether a price is an excessive price must determine if that
price is higher than a competitive price and whether such difference is unreasonable,
determined by taking into account all relevant factors, which may include—
(a)the respondent’s price-cost margin, internal rate of return, return of capital
invested or profit history;
(b)the respondent’s prices for the goods or services –
(i) in markets in which there are competing products;
(ii) to customers in other geographic markets;
(iii) (iii) for similar products in other markets and
(iv) (iv) historically;
(c)relevant comparator firm’s prices and level of profits for the goods or
services in a competitive market for those goods or services;
(d)the length of time the prices have been charged at that level;

3333
(e)the structural characteristics of the relevant market, including the extent of
the respondent’s market share, the degree of contestability of the market,
barriers to entry and past or current advantage that is not due to the
respondent’s own commercial efficiency or investment, such as direct or
indirect state support for a firm or firms in the market, and
(f) any regulations made by the Minster in terms of section 78 regarding the
calculation and determination of an excessive price.”
Prices charged by comparator firms
[125] The Complainants contended that some smaller firms were charging much lower
prices than the pathologists for the PCR test, in some instances as much as 70% lower.
They argued that these smaller firms suffered a cost disadvantage compared with the
Pathologists, because the smaller firms did not achieve the sales volumes necessary
to achieve the same volume-related cost savings as the Pathologists.
[126] The Pathologists pointed out that the Complainants do not (i) identify these smaller
firms or the prices that they charged; (ii) identify the period during what period they
were charging lower prices; (iii) identify the “local” markets in which the smaller firms
were charging the lower prices; (iv) indicate what the base cost was for these smaller
firms; (v) indicate how the price of “as much as 70% lower” than that charged by the
Pathologists was arrived at. The Pathologists submitted that such evidence, if it
existed, should be provided, subject to a confidentiality regime if necessary.
[127] We agree with the Pathologists on this point. The assertion by the Complainants is
purely conclusory, without any particularity as to any of the facts which are said to
underlie the conclusion. There do not appear to be any probabilities that support the
Complainants’ allegation.

3434
[128] At the hearing, the Complainants’ counsel accepted that this information would have
to be provided in due course, in order for the Complainants to be able to substantiate
this claim. However, at this stage of the pleadings, the identities of the smaller firms
could not be disclosed. There is no evidence before us that explains and justifies this
position.
[129] The Pathologists cannot meet and answer the complaint on the basis of this conclusory
and non-specific assertion.
[130] This ground of exception is therefore upheld. The Complainants are required to file a
supplementary founding affidavit to particularise its case with regard to the smaller
firms.
Reliance on the findings in the health market inquiry;
[131] The Complainants rely on the findings of the Health Market Inquiry report of September
2019 that the market for healthcare practitioners is characterised by high barriers to
entry. They state that the report expressed concerns at several features which serve
to benefit practitioners at the expense of patients and medical schemes. This has
created an environment where practitioners can increase prices and avoid innovation
without the threat of losing customers.
[132] The Complainants submit that the Commission’s Health Market Inquiry report finds
application in this case because the Pathologists did not face intense competition and
were not fearful of losing customers, which is evidenced by their ability to maintain their
prices over an extended period, despite a material decrease in their costs.
[133] The Pathologists contend that the Complainants have defined the market as the
market for PCR testing, and seek here to rely on another market. The Pathologists

3535
further contend that the market for the supply of PCR tests did not even exist in
September 2019, and therefore could have not have been the subject of any finding in
the Health Market Inquiry or in the Commission’s Final Report.
[134] The Pathologists further argue that the Complainants seek to rely upon, a very general
concern expressed by the Commission in the Inquiry regarding "a number of features
of the private healthcare market”, but not related specifically to pathologists. The
Complainants do not explain how a general finding relating to participation in tenders
is in any way relevant to an assessment of market power in the market that is relevant
to this complaint referral.
[135] Section 8(3) of the Act requires an assessment of whether the price in question is
higher than a competitive price and whether that difference is unreasonable, applying
the factors set out in section 8(3). These factors include the structural characteristics
of the relevant market. Paragraphs 67 to 68 of the Complaint sets out the basis for
referring to the report of the health market inquiry. The contentions raised by the
Complainants in this regard are somewhat speculative.
[136] It appears to us that this complaint is not a free-standing ground of exception. Rather,
it is a complaint that certain of the evidence on which the Complainants rely in support
of their complaint is irrelevant. That is a matter that can be determined at trial.
[137] Accordingly, to the extent necessary, this ground of exception is not upheld.
Unclear reliance on the “lucky monopolist” theory
[138] The Complainants assert that the Pathologists are in the position of a “lucky
monopolist.” They submit that the Pathologists offered PCR tests at a time when
demand exceeded supply, and customers were unwilling or unable to exert downward
pricing pressure on the pathologists. They contend that the Pathologists sought to

3636
profit from a most vulnerable group during a global pandemic and that this should
weigh against them.
[139] The Pathologists contend that if the Complainants wish to rely on the “lucky
monopolist” theory, they must plead facts to underpin the conclusion that the
pathologists by “sheer luck” gained market power.
[140] Further, Pathcare relied on the CAC’s decision in Babelegi, in which the following was
held:
[50] … in a crisis situation, such as that induced by the COVID-19 pandemic, one
needs to use a somewhat different conceptual framework from what ordinarily would
be employed in an excessive pricing case
… Recall however that the test for dominance for a firm that has less than 35% share
of the defined market is that it has market power; that is ‘the power to control prices or
to exclude competition or to behave in an appreciable extent independently of its
competitors, customers, or suppliers’. Within the context of this case, this definition
requires evaluation in terms of the cost, prices, and mark-ups prior to or during and
after the complaint period …”
[141] Pathcare submits that the Complainants have not undertaken an analysis of the cost,
prices and mark-ups of the PCR test of the kind that is required to substantiate a case
of the “lucky monopolist”.
[142] Pathcare further contends that the case of the “lucky monopolist”, as contemplated by
the CAC in Babelegi and the Tribunal in
Dis-Chem and Tsutsumani, is concerned with
a material price increase during a disaster, relative to what was charged pre-disaster,
and whether that increase could ultimately be justified by any cost increases. PCR

3737
tests for the detection of the COVID-19 virus were only introduced in South Africa after
the commencement of the disaster, in around March 2020.
[143] When the Tribunal hears the evidence, it will decide whether the Complainants’
allegations can be sustained. The Complainants have at this stage sufficiently set out
the material facts necessary for the Pathologists be able to answer.
[144] This ground of exception is therefore not justified, and it is dismissed.
Ninth ground of exception: Failure properly to plead detriment
[145] In their self-referral, the Complainants contend that PCR tests were a vital tool in
monitoring and reducing the spread of the virus. They contend that it is likely that as a
result of the Pathologists charging an excessive price, fewer PCR tests were sold than
would otherwise have been the case. According to the Complainants, the Pathologists'
conduct in this regard contributed to the spread of the virus.
[146] The Complainants further contended that the allegedly excessive price charged by the
Pathologists increased the cost of the claims made by scheme members, and reduced
the schemes’ reserves, which affected the members’ required level of contribution.
[147] Ampath submits that there is no factual basis for the contention that its pricing was in
fact detrimental to consumers or customers. It further submits that there is no factual
basis for the allegation that fewer tests were conducted than there would otherwise
have been. Ampath points out that the Complainants have not put up any facts that
demonstrate an overall increase in members’ claims or a reduction in reserves.
[148] Counsel for Lancet argued that the pleadings do not demonstrate actual detriment
suffered by the schemes. It was further submitted that the Complainants’ self-referral
is vague as it fails to set out the following information:

3838
148.1The actual prices that were paid to Lancet, the other respondents and the
“smaller firms” for the PCR tests and/or testing services;
148.2The number of PCR tests and/or testing services that they paid for;
148.3 The total value that was paid for the PCR tests and/or testing services in
respect of each of the respondents and the “smaller firms” over the relevant
period; and
148.4The actual effect that such payments had on the schemes’ reserves and
consequently on the level of contribution required.
[149] Counsel for Lancet further argued that the allegations pleaded do not distinguish
between consumers or customers. On the pleaded facts, it is not apparent whether it
is the Complainants or their members who are the customers and/or the consumers of
the PCR tests. Given the nature of the Complainants (a non-profit company and
medical schemes), it is not apparent how they were themselves consumers of PCR
tests. Lancet further argued that it is also not apparent how the members of medical
schemes were customers, where it is not alleged that they paid for the PCR tests. Nor
is it positively alleged that the level of contributions from members in fact increased as
a result of or linked to the cost of the PCR tests.
[150] In response, the Complainants contended that the charging of exorbitant prices for life-
saving goods or services in the context of the pandemic is by its nature detrimental to
consumer or customers. The Complainants relied on the CAC’s decision in Babelegi
There, the Court held that when Babelegi charged excessive prices, at a time of crisis
when the employment of a mask by every person in the country was seen as being
essential to the protection of the health, safety and welfare of others and therefore as
critical to the reduction of the danger posed by COVID-19, the high prices of such a
necessity “unquestionably acted to the detriment of consumers in the country”
5757
5757Babelegi CAC at para 67.

3939
[151] The Complainants submitted that the detriment was axiomatic on the facts of the case.
We agree. It is difficult to see how the charging of an excessive price for a necessity
could not be detrimental to those that received and paid for the services, whether
directly or indirectly. Whether it can be shown that this also resulted in a reduction in
the number of sales, contributing to the spread of the virus, remains to be seen.
[152] We consider that in paragraphs 75 to 79 of their self-referral affidavit the Complainants
sufficiently set out the alleged facts on which they rely. The Tribunal will after the
hearing of evidence decide whether the Complainants' allegations can be upheld. At
this stage, the Complainants have sufficiently set out the material facts necessary for
the pathologists to answer the allegations.
[153] This ground of exception is without foundation, and is dismissed.
[154] The Tribunal makes the following order:

4040
ORDER
Having read the papers and heard the exception applications brought by Dr Du Buisson,
Kramer, Swart, Bouwer Inc t/a Ampath (“Ampath”), Case No CRP102Oct23/EXC187Dec23,
Drs Dietrich Voigt, Mia and partners t/a Pathcare (“Pathcare”), Case No:
CRP102Oct23/EXC177Feb24, and Dr Mauff AC and Partners t/a Lancet Laboratories
(“Lancet”), Case No: CRP102OCT23/EXC143DEC23, the Tribunal makes the following order:
[1]The exceptions are dismissed save for the exception relating to the comparator firms’
prices.
[2]The Complainants must file a supplementary affidavit within 15 business days of the
date of this order, stating the following:
2.1. The names of the comparator firms;
2.2. The prices charged by these comparator firms;
2.3. The markets in which these comparator firms allegedly charged the much
lower price; and
2.4. The period in which these comparator firms charged the lower price.
[3]Lancet and Pathcare must file their answering affidavits within 20 business days of
receipt of the Complainants’ supplementary affidavit.
[4]Ampath must file its supplementary answering affidavit within 20 business days of
receipt of the Complainants’ supplementary affidavit.
[5]The Complainants may file a replying affidavit, if they so wish, within 10 business
days of the answering affidavits.
[6]There is no costs order.
19 February 2025
Adv Geoff Budlender SC Date
Ms Mondo Mazwai and Prof. Imraan Valodiacoconcurring.
Signed by:GEOFF BUDLENDER
Signed at:2025-02-19 15:31:45 +02:00
Reason:Witnessing GEOFF BUDLENDE

4141
Tribunal Case Managers: Nomkhosi Mthethwa-Motsa and Theresho Galane.
For the Complainants:
For Ampath:
Adv M Van Der Nest SC and Adv S Quinn instructed
by ENS Africa Inc.
Adv MJ Engelbrecht SC and Adv L Zikalala instructed
by Herbert Smith Freehills Inc.
For Pathcare:
For Lancet
For the Commission
Adv A Gotz SC and Adv L Buchler instructed by Janine
Nainkin Inc.
Adv M Le Roux SC, Adv C Avidon and Adv S Mbatha
instructed by Webber Wentzel Inc.
Simphiwe Gumede and Maribe Malope.