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Pharmacy Oversight and Supervision Requirements for Preparation of Licensed ATMPs
31 January 2020
·
This guidance provides definitions of oversight and supervision it clarifies where each are required when implementing ATMPs.
Off-label or unlicensed product use under HMR 2012 exemptions
8 January 2020
·
A legal position summary regarding the sale, supply or administration of off-label/unlicensed products under Schedule 17 of the Human Medicines Regulations 2012
Patient Group Direction use in Primary Care Networks
8 January 2020
·
Guidance on the legislation and governance required when considering the use of PGDs across a PCN
Registration required
Medical Gas Testing Register, April 2020
20 December 2019
·
Compiled and Maintained by NHS Pharmaceutical Quality Assurance Committee (Medical Gas Sub-Group) “Only individuals who have been appointed to the Quality Controller (MGPS) register may…
Multiple Use of Injectable Medicines in Clinical Areas V 02 February 2020
19 December 2019
·
This document is intended for multi-professional clinical practitioners to use as a reference and source of information for the prescribing, reconstituting or administering injectable medicines.…
Guidance on In Use Shelf Life for Eye Drops and Ointments
16 December 2019
·
This document takes a risk based approach to assigning the in- use shelf life for eye drops used in UK hospitals based on the risks…
Medicines Shortages and Patient Group Directions
16 December 2019
·
This article outlines how PGDs can be managed to allow for their continued use in cases of medicines shortages.
National Homecare Medicines Committee (NHMC) Homecare Risk Assessment
10 December 2019
·
To support organisations in establishing a robust risk assessment process for new homecare medicines services the NHMC has developed a tool for local use. …
When and how can dentists supply medicines?
28 November 2019
·
The attached Medicines Q&A aims to explain the legal status of medicines in the UK and when and how they may be supplied by dentists to patients
Supply of aseptically Prepared Doses of IMPs Across Legal Boundaries Version 2 October 2019
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…
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