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  • The Clinical Trial Study Protocol (Advanced)

  • Hosted By:
  • ComplianceOnline
  • Start:
  • Friday - Feb 22, 2013 10:00 AM
  • End Time:
  • Friday - Feb 22, 2013 11:15 AM
  • Location:
  • Online
  • This clinical study protocol training will discuss the key elements in a study protocol and help you ensure that your protocol is clearly defined and conforms to GDA GCP guidelines.

    Why Should You Attend:

    Study protocols are an essential component of Good Clinical Practice (GCP) regulations.

    In a clinical trial, the protocol is carefully designed to safeguard the health of the participants as well as answer specific research questions. A protocol describes what types of people may participate in the trial; the schedule of tests, procedures, medications, and dosages; and the length of the study.

    This session will train investigators and clinical research staff in the key elements of a clinical study protocol, the process of protocol development and the specifics of FDA obligations to help ensure data integrity and institutional compliance.
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