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Aithisgean ùra
Committee Reports
Aithisgean Chomataidh
Research Briefings
Brathan-ullachaidh Rannsachadh
Feedback
Ais-eòlas
Published by The Scottish Parliamentary Corporate Body
PE1517 - Polypropylene Mesh Medical Devices
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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
Membership changes
Introduction
Context of mesh issues
Publication of the interim report
Clinical studies completed after publication of the interim report
Publication of the final report
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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