North Central Florida: Fundamentals of Good Clinical Practice

When:  Jan 31, 2018 from 03:00 PM to 05:00 PM (ET)

Fundamentals of Good Clinical Practice (GCP)

Speaker: Wajeeh Bajwa PhD

Registration Cost: FREE and open for all to attend.

Program Agenda:
  • 3:00 PM – Registration & Networking
  • 3:15 PM – Welcome and Introductions
  • 3:20 PM – Educational Presentation
  • 4:45 PM – Questions and Answers
Program Description: A basic overview of FDA guidance and regulations that exist for conducting human subject research.

Upon completion of this session, attendees should be able to:
  • Review principles and regulatory requirements for Good Clinical Practice (GCP).
  • Discuss roles and responsibilities of the Principal Investigator and study’s staff, protocol compliance, and other criteria for conducting clinical trials.
  • Examine best practices, examples of GCP noncompliance, and corrective actions for protocol or procedural deviations.
  • Discuss compliance scenarios related to regulatory and protocol compliance.
Target Audience: Researcher Professionals involved in human subject research at UF Health and around North Central Florida

Contact hours: 1.5 Contact hours have been applied for through ACRP. Membership is not required for online registration of contact hours. JK

To receive contact hours: Purchase the contact hours, sign in at the registration desk, and attend the program. Log on to the ACRP website then “ACRP Learning Portal” to complete the evaluation no later than 30 days following the event and obtain the online certificate.

Contact Hour Cost:
  • $0 Chapter Members
  • $15 ACRP Members
  • $30 Non-Members
Refund Policy: No refunds unless the event is cancelled by the chapter.

Level: Intermediate

Further Information:
Contact Alie Trainor, MPH, CPH, CCRC
ACRP NCFL Chapter President


Online Instructions: