FDA Clinical Investigator Training Course (CITC) 2023
December 6 – 7, 2023
This course is designed to promote professionalism in the clinical trial industry for individuals involved with submissions to FDA (Investigational New Drug (IND) application, New Drug Application (NDA), Biologics License Application (BLA)), and to familiarize stakeholders with the regulatory and scientific issues involved in the development and approval of medical drugs and biological products.
Click Here for Workshop Details
The agenda is still being refined and may be updated over time. The current version is v3, uploaded on October 13, 2023.
The speaker biographies document provides detailed information for each of the presenters.
Download Presentation Slides:
Evaluation & Certificate:
Evaluation & Certificate of Attendance
Session Recordings:
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Continuing Education:
Real-time attendance is required for the certificate of attendance which can be used in support of CEs for the following professional organizations.
Certificates are only available during the two weeks post-event (until December 21, 2023).
This workshop has been approved for 9.75 contact hours of continuing education for physicians, pharmacists, and nurses. Please see the detailed announcement for more information. Each day after the course concludes, that day’s attendees will receive an email with instructions and a code to claim their credit. Only participants who attend the live broadcast via Adobe Connect will receive the claim codes.
This event has been pre-approved by:
- RAPS as eligible for a maximum of 12 credits for a two-day event (appropriate to real-time attendance) towards a participant’s RAC recertification upon full completion.
- SOCRA who accepts documentation of candidate participation in continuing education programs for re-certification if the program is applicable to clinical research regulations, operations or management, or to the candidate’s clinical research therapeutic area.
- SQA as eligible for 1 non-GCP or non-GLP unit for every 1 hour of instructional time towards a participant’s RQAP re-registration.
- ACRP for continuing education in clinical research. ACRP will provide 1 ACRP contact hour for every 45-60 minutes of qualified material.
Questions?
Please refer the FAQs page on this website. If you are not able to find your answer there, please email us at info@sbiaevents.com.
More Information
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