Manufacturer's Online Reporting Environment (MORE)

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Document information

A digital platform designed to facilitate the reporting, monitoring, and management of medical device incidents.

Adapted edition

Document type
Reference Guide
Format
DOCX
Pages
3
Language
English
Version
1.0
Updated
2026-09-17
Description

A digital platform designed to facilitate the reporting, monitoring, and management of medical device incidents. Consult the original guidance for current legal and operational details.

Contents
  • How to report to the MHRA
  • Great Britain (England, Scotland and Wales)
  • Northern Ireland
Source and licence
Manufacturer's Online Reporting Environment (MORE)

Medicines and Healthcare products Regulatory Agency

AttributionMedicines and Healthcare products Regulatory Agency, ‘Manufacturer's Online Reporting Environment (MORE)’ (updated 9 June 2025), reused under the Open Government Licence v3.0.

ChangesNeutral text-only adaptation from the official GOV.UK Content API body: headings, paragraphs, ordered and unordered list items and clickable source-link destinations in an appendix preserved. Images, logos, page design, accessible-format request widgets and linked attachments excluded; normalised whitespace, invisible format marks and typography.

Version history
  • v1.017/09/2026
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