Good Clinical Practices (GCP) - Understanding and Implementing the Current Global Requirements

Course "Good Clinical Practices (GCP) - Understanding and Implementing the Current Global Requirements" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.

    Defining the basic requirements of Good Clinical Practices
    Clinical Study Protocol Elements and Device Accountability
    Role of Institutional Review Board (IRB) and Informed Consent
    Principles of Ethics and Quality Control
    Determining the appropriate duties and oversight required of the sponsor, monitor, and investigators to ensure a high level of quality in a clinical trial
    Ensuring that quality practices are designed and implemented to guarantee compliant clinical trials
    Learning how to effectively manage a Sponsor, as well as, an FDA GCP inspection
    Developing mechanisms to uncover and preclude fraud and misconduct in clinical trials
    And Much More...