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Choosing between oral vancomycin options

18 May 2021Local decision makers should choose between the options for giving vancomycin orally. Licensing status and other factors affect decision making.

Repacking and over-labelling small batches of medicines

1 October 2020Smaller packs of licensed medicines can be produced for clinics and departments by their hospital pharmacy, under pharmacist supervision in accordance with GMP

Supplying contrast agents under a Patient Group Direction

12 August 2020Advice on the preparation and/or administration of contrast agents supplied under a Patient Group Direction (PGD).

Pharmacy Oversight and Supervision Requirements for Preparation of Licensed ATMPs

31 January 2020This guidance provides definitions of oversight and supervision it clarifies where each are required when implementing ATMPs.

Requirements for Governance and Preparation of Gene Therapy: Pan UK Pharmacy Working Group for ATMPs

30 October 2019Practical advice for centres implementing Gene Therapies detailing GMSC and Governance requirements and optimal preparation location.

Emergency Preparation of Eye Drops In Unlicensed Aseptic Units 1st Edition

18 September 2019This document aims to provide guidance to NHS Chief Pharmacists and Accountable Pharmacists working under the Section 10 exemption to the Medicines Act 1968 on…

Guidance on Definition of Supervision under Section 10 Aseptic Preparation Activities, 3rd Edition, Sep 2019 (Yellow Cover)

3 September 2019The NHS Aseptic Services Accreditation Working Group, working closely with the South West Product Approval Accreditation Programme have developed and published a definition of Supervision…

Standard Protocol for Deriving and Assessment of Stability - Part 5 Sterile Products

1 June 2017This protocol applies to small molecule products of all presentations, manufactured from non-sterile starting materials and sterilised in their final container.

A Standard Protocol for Derivation and Assessment of Stability Part 4 – Parenteral Nutrition

1 June 2017To support NHS compounding units and purchasers to derive and assess stability data for pharmaceutical products (Specials and extemporaneously compounded).

Standard Protocol for Deriving and Assessment of Stability - Part 2: Aseptic Preparations (Biopharmaceuticals)

6 March 2017Stability of the protein structure is an important feature in preserving the safety and efficacy of biopharmaceuticals.