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Supporting funding applications for CTIMPs

12 December 2022Sponsor pharmacy role in funding applications and establishing costs for sponsor activities

Transporting COVID-19 vaccines

19 August 2022

Monitoring and auditing clinical trials by participating sites

12 December 2022An overview of the Sponsor Pharmacy's responsibilities for monitoring and auditing a clinical trial as part of participating site management

Closing clinical trials

12 December 2022Sponsor pharmacy responsibilities during trial closure and the final monitoring visit

Supply and administration of medicines by staff group (P to Z)

2 April 2024

Use of PGDs by trainee registered healthcare professionals

8 September 2020This article outlines the advice on the use of PGDs by registered healthcare professionals who are undertaking training and/or competency assessment.

Use of individually named medicines in HM Prisons

9 June 2022Advice on the use of individually named patient supplies versus stock medication for residential custodial settings

Understanding the characteristics of COVID-19 Vaccines

19 August 2022An introduction to the Understanding the characteristics of COVID-19 Vaccines pages

Risk assessing Investigational Medicinal Products (IMPs)

12 December 2022Sponsor pharmacy responsibilities when assessing the risk associated with CTIMPs

Regulatory requirements for export of ATMP starting materials: Pan UK Pharmacy Working Group on ATMPs

27 September 2019Regulatory export requirements for hospitals procuring (harvesting) patient’s own cells/tissues for use as starting materials in the manufacture of ATMPs.