27 September 2019 · Regulatory export requirements for hospitals procuring (harvesting) patient’s own cells/tissues for use as starting materials in the manufacture of ATMPs.
21 June 2021 · Moving vaccines within and between organisations is subject to regulatory constraints. Senior pharmacists need to be able to advise on appropriate practice.
20 January 2021 · Summary The 2020 version of the retention of pharmacy records document is now available. Purpose This document, based on one first generated at the request…
16 December 2016 · The purpose of this document is to give guidance to those outsourcing PN compounding on the risks in the outsourcing and supply process and to…
11 November 2019 · 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…
21 January 2019 · This guidance will be of use to anyone purchasing, overlabelling or supplying imported
unlicensed medicines, and obtaining or providing translated leaflets.
8 September 2020 · This Q&A outlines the advice on the use of PGDs by registered healthcare professionals who are undertaking training and/or competency assessment.
17 September 2004 · The Medicines Act 1968 introduced a licensing system to regulate the manufacture, distribution and importation of medicinal products. Section 10 of the Act exempts pharmacists…
28 November 2019 · This updated Medicines Q&A aims to explain the legal status of medicines in the UK and when and how they may be supplied by dentists…