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

RQA Member: USD ($) 137.00
Non-Member: USD ($) 178.00

Your Price: USD ($) 178.00


Please note payment is required before access is given. However, if you need earlier access to the eLearning please contact elearning@therqa.com.

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 completed the assessment (80% pass mark), you will be shown your pass mark and percentage and will then be asked to complete your details to generate a PDF certificate (displaying the CPD points gained) which you can download or print for your records.

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.

CPD Points

4 points

Course Demo

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

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