Good Manufacturing Practice - the Essentials

1 Day/s

CPD Hours: 7

Online, in-house, e-learning

This interactive course examines why we have Good Manufacturing Practice (GMP), its legal status and the key GMP issues surrounding pharmaceutical manufacture such as documentation, training and facilities. This informative course introduces the EU Guide to GMP and considers its implementation in the modern pharmaceutical regulatory environment.


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This course is suitable for all pharmaceutical professionals, including newcomers to the industry, who wish to gain a solid knowledge and understanding in the essentials of pharmaceutical GMP.

This course covers the following topics:


  • Expectations of medicines
  • Why do we have GMP? What’s involved?
  • Pharmaceutical quality system
  • The EU guide to GMP and the US CFRs
  • GMP - who is involved? Roles of key personnel and their departments
  • Documentation - what are the GMP requirements?
  • GMP in the warehouse and dispensary
  • GMP in production and packaging
  • People and training
  • Introduction to deviations

In addition, the course includes a number of interactive exercises

    By the end of the course you will be able to:


    • Find your way confidently around the EU Guide to EU GMP and how it is applied in the UK as the Orange Guide
    • Understand the expectations of current good manufacturing practices, and how these can be achieved at a practical level in the manufacture of pharmaceutical products
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Helping your training budget go further

We offer a number of discounts and specials offers on our training courses including Group booking, NHS and Seasonal discounts.

Meet the tutors

Rob Hughes

Rob Hughes has over 30 years in the pharmaceutical industry spanning various operational, project and senior strategic leadership positions in commercial manufacturing and development QA. Rob, a practising QP, has experience of the application of QA in many different areas including control laboratories, API, solids, creams and liquids manufacture, and third party audit and evaluation. Rob has many years experience of MHRA and FDA inspections.

Leo Goodchild

Leo is a pharmaceutical professional with over 20 years of experience across the industry and is currently RSSL’s Training & Development Specialist. He is an experienced L&D professional with a broad depth of knowledge as a trainer, coach, and mentor. He has helped many people on their way to successful career paths.

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