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Southeast Louisiana: FDA Inspections of Clinical Investigators
Nov 16, 2017 from 06:00 PM to 09:00 PM (CT)
ACRP Gulf States Chapter
FDA Inspections of Clinical Investigators
No cost for Chapter Membersm ACRP Members or Non-Members
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
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
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
Clinical Researchers & ACRP members
911 Harrison Avenue
New Orleans, LA 70124
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