GSK: Responsive disease-awareness website breached Clause 8.3 due to uncertified desktop vs mobile final forms (AUTH/3819/9/23)

📅 8 March 2026 | 🖉 Dr Anzal Qurbain
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Key facts

CaseAUTH/3819/9/23
CompanyGSK UK Limited
ComplainantAnonymous, non-contactable
MaterialGSK “Tackle Meningitis” disease awareness website (public educational material)
Main issueDesktop and mobile views differed; Panel considered these to be substantively different final forms requiring separate certification
Pages assessedHomepage; “Know the symptoms” webpage
Applicable Code year2021
Breach findingsClause 8.3 (x2)
No breach findingsClause 5.1; Clause 2
SanctionsUndertaking received; additional sanctions not stated
Complaint received7 September 2023
Case completed7 November 2024
AppealNo appeal
Sourcehttps://www.pmcpa.org.uk/cases/completed-cases/auth3819923-complainant-v-gsk

Download the full case report (PDF)


Reviewed by Dr Anzal Qurbain (FFPM) — ABPI Final Signatory

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What happened

  • An anonymous, non-contactable complainant alleged GSK’s public disease-education website (Tackle Meningitis) had not been certified separately for mobile viewing.
  • The complainant pointed to differences between desktop and mobile views on: (1) the homepage and (2) the “Know the symptoms” webpage.
  • Examples cited included icons appearing on mobile tiles but not desktop, and content/tabs present on desktop but not on mobile.
  • GSK said the site was “responsive” (one website adapting to screen size) and stated it had been reviewed/approved on desktop and mobile via a staging environment, with evidence recorded in its approval system.
  • The Panel assessed whether the differences created two different “final forms” and whether each had been certified as required for public disease education material.
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Outcome

  • Breach of Clause 8.3 (x2) – failing to certify educational material for the public related to disease (for each of the two webpages assessed).
  • No breach of Clause 5.1 – requirement to maintain high standards.
  • No breach of Clause 2 – activities/materials must not bring discredit upon, or reduce confidence in, the pharmaceutical industry.
  • No appeal.
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