GMP Intermediate course

This course gives you a comprehensive review of GMP compliance requirements and tools to master application and interpretation of these requirements. This course is aimed to take you further in your understanding of GMP requirements and will assist you in your daily challenges either working in QA or with GMP related tasks in other parts of a pharmaceutical operation.

Course description

The course is split into a preparatory session for you to do online at your own convenience followed by a 2-day intensive masterclass led by our highly experienced trainers. During these two days, you will get an overview of requirements in both EU and US GMP as well as a number of practical class exercises. You will learn to understand, navigate, interpret and apply GMP in line with up-to date views on ICH guidelines on Pharmaceutical Quality System and Quality Risk Management.  

The course material will include references to specific requirements, guidelines and interpretations from authorities and regulatory associations. 

Course outline

• Preparatory session – How to read and interpret the GMP texts (on-line and on-demand)
• Introduction
• The foundation for GMP-requirements
  • How R&D impacts the application of GMP in manufacturing
• GMP and risk management
• Process and production controls
• Material controls
• Personnel
• Document controls
  • Including data integrity
• GMP in the product life cycle
  • Maintaining control
  • Change management
• If control is lost
  • Deviations, complaints, CAPA
• Quality Management System
  • Quality Culture
  • Responsibilities
• Summary

Learning objectives

After this course, you will have a full overview of the contents of both EU and US GMP. You will also be able to distinguish between requirements, interpretations and industry practice. You will be equipped with tools and strategies to navigate the universe of GMP guidance documents and have enhanced your ability to apply current GMP requirements to potential challenges in the daily operations of a GMP environment.

Who should attend

The course is suitable for persons working with development, production, or QA who is involved in, or responsible for the operation or audit of pharmaceutical quality systems including GMP. Also those who need more knowledge about specific FDA requirements where these differ from EU GMPS will  benefit from this course.

Prerequisites

• You should have basic knowledge of GMPs, e.g. by participating in one of our basic courses or have equivalent knowledge.
• You should have at least 6-12 months experience of working in the regulated industry (Pharmaceutical manufacturing).

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