North Central Florida: Good Clinical Practice Training

When:  Jul 24, 2020 from 12:00 PM to 01:30 PM (ET)

Good clinical practice training

Please click here to purchase contact hour.

Speaker:
Sheila Austin, MS, MSE, CIP - Regulatory Specialist, University of Florida 

Program Agenda:
  • 12:00: Welcome and Introductions
  • 12:05 - 1:15: Presentation and Discussion
  • 1:15 - 1:30: Question and Answer Session
  • 1:30: Closing Remarks
Program Description: This program will discuss the history of GCP, the relationship between GCP guidelines and FDA regulations, and dive deeply into the principles of GCP and study team responsibilities. This is an interactive presentation, participants will be asked to engage in discussing scenarios that test our knowledge and interpretation of GCP principles.

Upon completion of this session, attendees should be able to:

  • Identify key historical events that led to the development of GCP standard
  • Discuss the relationship between UF FDA regulations and GCP
  • List the core principles upon which GCP is based.
  • Describe Investigator Responsibilities under GCP
Contact hours: 1.5 Contact hours have been applied for through ACRP. Membership is not required for online registration of contact hours.

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.

Registration Cost:
  • $0 for all attendees
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

Location

Dial-in Instructions: