Service advice and planning
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Supervision of aseptic preparation under Section 10 exemption
17 November 2025The section 10 exemption from the Medicines Act permits aseptic preparation of medicines under the supervision of a pharmacist.
Legal mechanisms to supply and administer medicines to individuals
1 April 2026The main legal mechanisms used to supply and/or administer medicines are explained and considerations suggested for the most appropriate option(s)
Monitoring and auditing clinical trials
29 April 2026An overview of the Sponsor Pharmacy's responsibilities for monitoring and auditing clinical trial locations.
Closing clinical trials
29 April 2026Sponsor pharmacy responsibilities during trial closure and the final monitoring visit
The role of the sponsor pharmacy in clinical trials of investigational medicinal products (CTIMPs)
30 April 2026Identifying key areas where pharmaceutical expertise is required by sponsors for conducting non-commercial clinical trials
Supporting funding applications for CTIMPs
30 April 2026Sponsor pharmacy role in funding applications and establishing costs for sponsor activities
Assuring the supply chain for IMPs and NIMPs
29 April 2026Sponsor pharmacy role regarding the supply assurance of Investigational Medicinal Products (IMPs) and Non-Investigational Medicinal Products (NIMPs) in CTIMPs.
Feasibility and setting up of clinical trials at delivery locations
29 April 2026An overview of the Sponsor Pharmacy's responsibilities during setup of a clinical trial in a delivery organisation or location.
Exagamglogene autotemcel (Casgevy®)
13 February 2026This document highlights key areas where Chief Pharmacists should focus pharmaceutical expertise prior to implementation of exagamglogene autotemcel.
In-vivo GMO gene therapy medicinal products
13 February 2026This document outlines key areas for focus of pharmacy expertise prior to an organisation implementing in-vivo genetically modified organism (GMO) gene therapy.