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  • Overview of the OVCR Quality Improvement Program (QIP) PPT | PDF

  • Supervisory Responsibilities of Clinical Investigators PPT | PDF

Investigators are expected to follow GCP, and this training program will help you understand and comply with these standards.

By the end of this course you will:

  • Understand how regulations and guidelines protecting human research subjects came into being
  • Understand the Thirteen Principles of Good Clinical Practice
  • Understand the expected standards for informed consent
  • Understand how communication and proper reporting helps ensure the subject's rights, safely and well being.

To receive credit (2 credits):After completing the course, send email to oprstraining@uic.edu. OPRS will confirm completion.

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Web site: http://www.uictraining.org

 

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