This 4 day workshop has been developed specifically for Clinical Research Scientists that are fairly naïve to clinical research. The workshop will provide a platform from which delegates will gain an understanding and appreciation of the clinical research process and in particular the role and responsibilities of the monitor. With a strong focus on the ICH GCP requirements for monitoring, the primary objective of this course is to equip the delegates with the tools and knowledge to able to confidently select, initiate, monitor and close investigative sites in accordance with ICH GCP requirements.
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