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ICH-GCP Training

European Centre for Clinical Research Training (ECCRT)

28.11.2013; Brussels, Brussels, Belgien

contenido de curso

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.

objetivos de formación

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

destinatario

This course is designed for everyone who wants to understand the essentials of current regulations and GCP in clinical studies

oportunidad de trabajos y los campos profesionales mas buscados por personas ya tituladas

Any position in Clinical Research

certificación

ISO 9001:2008/ Q-for

Duración
1 Tage
Idioma
Englisch
Costos

EUR 750,00

Información e inscripción

Veerle Bultinck, E-Mail: veerle.bultinck@eccrt.com

 
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