Southeast Louisiana: FDA Inspections of Clinical Investigators

When:  Nov 16, 2017 from 06:00 PM to 09:00 PM (CT)
Associated with  ACRP Gulf States Chapter

FDA Inspections of Clinical Investigators

Registration Cost: No cost for Chapter Membersm ACRP Members or Non-Members

Program Agenda:
  • 6:00 – 6:30 pm – Registration & Networking
  • 6:30 –7:30 pm – Educational Presentation
  • 7:30 – 8:30 pm – Q&A
  • 8:30 – 9:00 pm – Networking 1:1 with speaker
Program Description: A presentation by Barbara Wright discussing the purpose & scope of FDA Inspections for clinical investigators. The learning assessment planned is a Q & A session post the presentation

Upon completion of this Webinar, attendees should be able to:
  • Understand the Authority, Purpose and Scope of FDA Inspections of Clinical Investigators
  • Understand the Principal Investigator obligations in Good Clinical Practice and Human Subject Protection regulations
  • Identify Most Common Deficiencies cited during FDA Inspections
  • Identify possible Enforcement Actions
Contact hours: 1.0 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.

Contact Hour Cost:
  • $0 Chapter Members
  • $15 ACRP Members
  • $30 Non-Member
Target Audience: Clinical Researchers & ACRP members


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