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Registration required
Carboplatin: Cytotoxic Drug Stability Monograph
24 August 2020
·
Stability information is essential for the safe aseptic preparation of carboplatin
Registration required
Cyclophosphamide: Cytotoxic Drug Stability Monograph
24 August 2020
·
Stability information is essential for the safe aseptic preparation of cyclophosphamide
Registration required
Dacarbazine: Cytotoxic Drug Stability Monograph
24 August 2020
·
Stability information is essential for the safe aseptic preparation of dacarbazine
Supply of aseptically Prepared Doses of IMPs Across Legal Boundaries Version 2 October 2019
11 November 2019
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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…
Guidance on Definition of Supervision under Section 10 Aseptic Preparation Activities, 3rd Edition, Sep 2019 (Yellow Cover)
3 September 2019
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The NHS Aseptic Services Accreditation Working Group, working closely with the South West Product Approval Accreditation Programme have developed and published a definition of Supervision…
Measurement of HEPA filter performance using the dispersed oil particle aerosol test for leak detection in filter installations ed 3
20 December 2018
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This test protocol is supplementary to Quality Assurance of Aseptic Preparation Services, Fifth edition, Edited by Alison M Beaney, Pharmaceutical Press, 2016.
Making best use of restricted aseptic compounding capacity
18 September 2018
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The NHS is experiencing considerable challenges regarding the supply of aseptically prepared injectable medicines. This communication from NPSG advises all NHS customers of commercial aseptic…
Guidance on Handling of Injectable Cytotoxic Drugs in Clinical Areas in in NHS Hospitals in the UK (Yellow Cover) Edition 1 July 2018
31 July 2018
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Intended audience: This document is intended as a reference and source of information to the following audiences: Nursing staff who handle cytotoxic chemotherapy (Oncology /…
Standard Protocol for Deriving and Assessment of Stability - Part 5 Sterile Products
1 June 2017
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This 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 2017
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To support NHS compounding units and purchasers to derive and assess stability data for pharmaceutical products (Specials and extemporaneously compounded).
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