GMP mid-level

This course gives answers to the question of which regulatory aspects are important throughout the product development cycle. What are the GMP requirements at various stages of product development (research, animal studies, clinical phases I, II & III)?

1 day
Course fee
€ 895 (excl. VAT)

Short description

This is a modular designed training wherein various GMP issues that are important for the development process of biopharmaceutical products are dealt with.

The training "GMP in Biopharmaceutical Development - From lab table to clinic" is presented in 2 modules that can also be followed seperately:

  1. Module 1: GMP mid-level (1 day).
  2. Module 2: GMP in Biopharmaceutical Development (2 days). You can read more about the second module of the course here

Module 1

Module 1 is about GMP: a standard for the production/analysis of medicines including the preparation/analysis  of clinical test material (Investigational Medicinal Product - IMP).

It is also important for companies to have knowledge of GMP during their research phase. On one hand these companies must deliver products that will be produced/tested under the GMP system at a later stage and, on the other hand, GMP is a quality control system and certain features of such a QC system are also applicable within a research environment.

The subjects to be discussed are:

  • Introduction to GMP - the regulations
  • Documentation
  • Deviations
  • OOS
  • Change Control
  • Quality Systems
  • Facility 
  • Equipment
  • Outsourcing work


  • Gaining understanding and knowledge of GMP
  • Understanding the importance of process flows and structures within the GMP system
  • Having practical and simple reference points to enable implementation of these systems within R&D

Target group

This training is developed for people who work within an R&D environment (laboratory/ production) who would like to know more about GMP, for example, to be able to adapt and adjust their development processes in accordance with future demands.

It will also be useful for those staff who work in an R&D oriented company that make or play a role in the manufacture and/or analysis of clinical material.

The training is also most suited to those staff who just want to know more about GMP or work in a pharmaceutical company but have not (yet) worked under GMP conditions.


Day 1



GMP introduction
Deviations & OOS,
Change control
Facility & Equipment
Outsourcing work



Workshop risk assesment
Set up a quality control system within an R&D environment
Carry out deviation research


Close out & Evaluation

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Interested in signing up a group of people for this course?

Please contact our Business Development team:
+31 (0)88 2830100

Need help? Have a question or a suggestion maybe?

Drop us a line below or call us on
+31 (0) 88 283 01 00.