ICH-GCP Training
28.11.2013; Brussels, Brussels, Belgien
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.
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
This course is designed for everyone who wants to understand the essentials of current regulations and GCP in clinical studies
Any position in Clinical Research
ISO 9001:2008/ Q-for
Veerle Bultinck, E-Mail: veerle.bultinck@eccrt.com