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Date : Monday, 02 July 2018
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ICH-E6 (R2) Good Clinical Practice Training

Health - Trainings
Date: Tuesday, 03 July 2018 10:00 - 17:00

Venue: Marcel Broodthaersplein 8/5, 1060 Brussels  |  City: Bruxelles, Belgium


The course will allow professionals who are active in clinical research to fully understand the requirements and responsibilities of everyone involved in clinical research.




Without training on the International Conference on Harmonization Good Clinical Practice (ICH-GCP) standards, or without experience in clinical research, professionals are not always aware of the legal regulations that govern clinical studies, including post-marketing trials. ICH-GCP is the guideline ruling all clinical research including its conduct, performance, monitoring and reporting of the results. This course focuses on the requirements of Good Clinical Practice (GCP) in clinical studies with pharmaceuticals. The complete and most recent version of the ICH-GCP is covered by this training, including the Addendum of 2016. All elements of the addendum, such as risk-based quality management and supervision will be presented. In addition, implementation of GCP requirements is explained and illustrated using examples from practice.



Furthermore, our ICH-GCP training meets the Minimum Criteria for ICH GCP Investigator Site Personnel Training Identified by TransCelerate BioPharma, as requested for mutual recognition of GCP training among trial sponsors.


+32 2 892 40 00
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Place Marcel Broodthaers / Marcel Broodthaersplein 8, South Center Titanium, 4° & 5° floor
1060 Bruxelles, Belgium




All Dates

  • Tuesday, 03 July 2018 10:00 - 17:00

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