Service advice and planning

Validation Master Plan 1st edition (Yellow Cover)

25 May 2010The Validation Master Plan (VMP) is a summary of the planned validation activities. It lists those activities and essential documents which will be generated and…

Use of PGDs by trainee registered healthcare professionals

8 September 2020Advice on the use of Patient Group Directions by registered healthcare professionals who are undertaking training and/or competency assessment

Understanding local governance in CTIMPs

12 December 2022Sponsor pharmacy's role in ensuring appropriate local governance arrangements for CTIMPs

Understanding iQAAPS

13 January 2023An introduction to the iQAAPS system, with information on how to access the system, find training resources and support contacts

Understanding essential documentation for clinical trials submissions

8 December 2022Sponsor responsibilities for writing and maintaining essential documents required for Clinical Trial Authorisation applications

The role of the sponsor pharmacy in clinical trials of investigational medicinal products (CTIMPs)

12 December 2022Identifying key areas where pharmaceutical expertise is required by sponsors for conducting non-commercial clinical trials

The Responsibilities of Chief Pharmacists for Radiopharmaceuticals (Yellow Cover)

28 April 2017Chief Pharmacist responsibilities with respect to radiopharmaceuticals have come more to the fore recently as a result of changes to the Ionising Radiation (Medical Exposure)…

Supporting funding applications for CTIMPs

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

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

2 April 2024Different staff groups have different permissions with respect to medicines supply and administration and it is important to ensure legislation is followed.

Supply and administration of medicines by staff group (H to O)