Fundamentals of Clinical Trials

Product ID : FCT16
Price: $60.00
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Through cancer clinical trials, researchers test the effects of new drugs on a group of volunteers with cancer. Following a strict protocol and using carefully controlled conditions, researchers evaluate the drugs under development and measure the ability of the new drug to treat cancer, its safety, and any possible side effects. Modeled after the ASCO International Clinical Trials Workshops, this CME and MOC accredited Program is designed to assist beginning investigators to familiarize themselves with the best practices of designing and conducting independent clinical research. Topic areas include: Research design/methodology, regulatory/legal issues, data management, ethical issues, statistics, research teams, exemplary clinical trials sites, and promoting clinical trials. Learning Objectives: Describe clinical trial methodology; Apply best practices in the implementation of research programs; Evaluate the roles and responsibilities of research team members; Communicate with patients the values of clinical research. The 2016 program update includes an all-new module on Informed Consent.

IMPORTANT NOTE: This course expires on June 29, 2019. Participants must complete all necessary course components by this date.

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