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…
The procurement specialists in England have formed the National Procurement Pharmacist Specialists Committee (NPPSC) which has produced a number of documents. This paper explains the rationale…
This updated Q&A aims to explain controlled drug legislation relevant to primary care dental practice. Includes prescribing for NHS and private patients, ordering/requisitioning, storage and…