This document provides guidance and advice which is still relevant to the NHS today, on the application of the licensing provisions of the Medicines Act…
The Medicines and Healthcare Products Regulatory Agency (MHRA) has sought legal advice and has confirmed that local authorities cannot delegate responsibility for organisational authorisation of…
This publication is a brief good practice guide for staff working in NHS commissioned health and social care organisations in England. It describes the legal…
The European Commissionfor medicinal products for human use has published version 9 of their Q&A on safety features on their website. This new version includes…
This document has been developed by the NHS Quality Assurance Committee and National Pharmacy Clinical Trials Advisory Group with input provided by the MHRA Clinical…
MHRA issues a monthly newsletter which is available only by email request to FMD.safetyfeatures@mhra.gov.uk. MHRA will also answer questions about FMD through this dedicated mailbox. Please send queries…
This guideline provides good practice recommendations for individual people and organisations involved with PGDs, with the aim of ensuring patients receive safe and appropriate care…
The MHRA publish information on the licences they have issues for medicines and also when they expire. This information has been collated and sorted into…