Law & Admin 2025 Online
27 - 29 Oct - Online Instructor Led
By the end of this module, you will have knowledge of the structure and application of current and forthcoming UK and EU legislation relating to the manufacture, control, storage, and supply of medicinal products (Human, veterinary, IMP for clinical trials)
It must be noted that delegates will need to maintain and apply their knowledge to fully meet the requirements of the UK QP Study Guide
The structure, content and administration of Marketing and site authorisations (MA, MIA, WDA or equivalents)
The role of the UK and EU Regulatory / Licencing bodies (MHRA/VMD/EMA) including procedures for defect reporting
Import and Export requirements for medicinal products
The impact of trade and recognition agreements on import / export requirements
The role of ICH and PIC/s
Regulations related to Pharmacovigilance and drug safety monitoring
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