description
Key Benefits of Attending this Course: • Understanding the principles underlying GCP and its specific rules of conduct • Achieving an overall understanding on how to conduct GCP compliant clinical trial • Evaluate the Investigator Responsibilities in Relation to regulations and ethics • Master effective clinical research documentation, from protocol development to final reporting and publication of results • Learn why Good Laboratories Practice would make a good requisite to GCP • Address the roles and responsibilities of inspectors, sponsors and auditors and how they affect your SOP • Discover quality assurance strategies for clinical operation excellence