ICH-GCP Training

European Centre for Clinical Research Training (ECCRT)
15.10.2014  Brussels, Belgium
20.01.2015  Brussels, Belgium
02.04.2015  Brussels, Belgium
22.09.2015  Brussels, Belgium
10.12.2015  Brussels, Belgium
Course Content
This concise course is designed for professionals who are active in clinical research. Without training on the International Conference on Harmonisation 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.
Learning objectives, training objectives
comprehend the basics of GCP requirements in clinical research and how they are implemented - understand the fundamentals of current legal regulations and guidelines - understand the essential documents of clinical studies
Target Audience
This course is designed for everyone who wants to understand the essentials of current regulations and GCP in clinical studies
Typical postgraduate careers and job opportunities
Any position in Clinical Research
ISO 9001:2008/ Q-for

Enquiries and Registration:

Ms. Sunita Kelecom
Clinical Research
1 day
EUR 750,00
Organizer contact info
Marcel Broodthaers plein 8b5
1060 Brussels
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