QP IMP/Clinical Trials 2025 Online
24 - 26 Feb - Online Instructor Led
By the end of this module, you will have an understanding of the requirements for manufacture, control, and distribution of Investigational Medicinal Products (IMP)
Understanding of the requirements and implementation of UK and EU legislation for IMPs, including Clinical Trial Regulation 536/2014 and its knock on effects to Good Manufacturing Practice
Knowledge and understanding of the regulatory structure of the Clinical Trial Application, including the IMPD, and Product Specification File
Understanding of clinical trial design, the impact of the different clinical trial phases on design and manufacturing and the ethical requirements for conducting trials in human subjects (Good Clinical Practice) including safety reporting requirements
How a risk based approach is applied to development and application of manufacturing, and control parameters for IMP, including levels of validation required for processes
Your materials, assignments and assessments will all be provided through this learning portal
You will be notified by email when items are available for you to access...
1 month before the course start date
~ You can access your course workbook
~ You will be able to download your Preparatory Assignment
Day before course start date
~ Downloads for workshops and exercises
End of each course day
~ Answers to exercises where appropriate
After course
~ Learning assessment
~ Course evaluation
~ Certificate
You will each be sent an invite to join the course via Teams
Call us directly on
01622 477781
email us
[email protected]
or pop your email in the box below and we will get right back to you