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PE1517 - Polypropylene Mesh Medical Devices
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PDF Published: Tuesday 21 Aug 2018
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  •  Overview
  •  Report
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  • Overview
  • Report
    • Membership changes
    • Introduction
    • Context of mesh issues
      • Role of the MHRA
      • Litigation and global concerns
    • Publication of the interim report
      • Evidence from chair of the Independent Review
      • Minority report
      • Scottish Government position on interim report recommendations
    • Clinical studies completed after publication of the interim report
    • Publication of the final report
      • Recommendations of the final report
      • Resignations from the independent review
      • Evidence from the Chair of the review and the Scottish Government
      • Process for agreeing and publishing the final report
        • Chapter 6
        • Mandatory reporting of mesh adverse events
        • Inclusion of petitioners' contributions in the final report
        • Classification of mesh devices
        • Expert clinician evidence - Dr Wael Agur
        • Petitioners' evidence
    • Professor Britton's review
    • Conclusions and recommendations
    • Annexe A - Extracts from Minutes and links to oral evidence
    • Annexe B - Written evidence submitted to the Committee
    • Annexe C - Conclusions and recommendations of the Independent Review’s interim report
    • Annexe D - Conclusions and recommendations of the Independent Review’s final report
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Last Updated: 20/5 7:38pm

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