Location:

This course takes place in Oxford, England.

Description:

This course aims to provide delegates with an understanding of GMP requirements for IMP and practical guidelines for ensuring GMP is followed at site

Who it is suitable for:

The course is aimed at anyone involved in the supply and management of IMP for investigational sites. For example, CTAs, CRAs, Project Managers, Pharmacists, Investigators.

Example Content:

Background

• Documents
• Regulatory and Advisory Bodies
• Definitions

Annexe 13

• Content
• Implications

New EU Guideline on IMPs and Non-IMPs

• Content
• Implications

Requirements for Manufacturing