Learn Good clinical Practice and related regulations

You will benefit from this course if you are involved in regulatory affairs, statistics and data management, compliance,  clinical research, clinical operations and quality assurance among others

The purpose of this course is to improve your knowledge relating to the conduct of clinical trials in humans subjects. The differences and similarities between Canadian regulations and the ICH Good Clinical practices will be highlighted. The role of the sponsor, monitor, investigator, research ethics board will be discussed. Essential clinical trial documents such as protocols, informed consent and investigators brochure will also be presented.
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