Title of the course: Good Clinical Practice Training
Upon completion of this online course trainees will:
To understand the basics of Good Clinical Practice and the current legal regulations and guidelines;
have the confidence to identify and describe the main responsibilities of the IRB/IEC, the investigator, the sponsor and the monitor;
get familiar with the essential documents related to GCP and understand the essence and purpose of important trial related files such as the informed consent forms, the investigator’s brochure and the clinical trial protocol.
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