Introduction to Good Manufacturing Practice (GMP) for Investigational Medicinal Products elearning

RQA Member: USD ($) 375.86
Non-Member: USD ($) 112.55

Your Price: USD ($) 112.55

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Course Introduction

This online course provides an introduction to Good Manufacturing Practice for Investigational Medicinal Products. The course is divided into the following ten bite size learning Modules

• Events leading to the introduction of Good Manufacturing Practice 
• The evolution of the Good Manufacturing Practices      
• Regulations around the world
• Understanding the basic principles of Good Manufacturing Practice within a research & development context
• Overview of the EU Good Manufacturing Practices (Part 1)
• Overview of the EU Good Manufacturing Practices (Part 2)
• The EU Good Manufacturing Practice annexes
• Annex 13: Investigational Medicinal Products
• The role of the Qualified Person
• Additional resources

Each bite-size module is around 30 minutes in duration and includes self assessment to confirm your gained knowledge.

Certificate

Once you have successfully passed the assessment (80% pass mark) you will receive a certificate in PDF format for your records. Please note that you will not have immediate access to this assessment.​

Author

Paul Last is a former Chairman of both RQA and the RQA GMP Committee. He previously worked at Pfizer Global Research & Development (PGRD) as vice president of the global supply chain responsible for the manufacture of active pharmaceutical ingredients and investigational medicinal products, IMP packaging, labelling and distribution. 

Corporate Licences

Multi-user licences for corporate use are also available, please click here for prices and further information.

Course Demo

Click here for demo (website registration/login required).

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