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Clinical Research — Clinical Trials and GCP

Complete Clinical Research and Good Clinical Practice (GCP) course. You will study clinical trial phases, protocol design, ICH GCP (E6 R2), FDA and EMA regulation, clinical data management (CDISC, SDTM, ADaM), biostatistics, trial monitoring and management, audit and inspections, ethics committees and informed consent. The course includes preparation for ACRP CRA (Clinical Research Associate) certification.

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