FDA Clinical Investigator Training Course (CITC) 2024
December 10-12, 2024
The primary goal of this clinical investigator training course is to provide participants with the essential knowledge and skills to conduct clinical trials effectively, ethically, and in accordance with regulatory standards. The course aims to prepare clinical investigators to conduct high-quality research that contributes to scientific knowledge and improves patient care.
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The agenda is still being refined and may be updated over time. The current version is v5, uploaded on October 15, 2024.
Speaker Biographies
The speaker biographies document is under development and will be linked here when it is ready.
The links below will become active on the day of the workshop.
Login One
Attendance is tracked for CE.
Ability to submit questions, but cannot pause or rewind
1,000 seats – Use Login Two if this room is full
Login Two
Attendance is tracked for CE.
Ability to submit questions, Ability to pause or rewind
Unlimited Seating
Livestream Direct
Attendance IS NOT TRACKED for CE.
If you encounter issues with the above logins, us this link.
The above login rooms will open ~15 minutes before each day begins.
If you encounter any technical issues, visit the Technical Issues Support Page
The audio for the event will be provided through your computer speakers (there will NOT be a teleconference number to dial into).
Download Presentation Slides:
ZIP of the CITC Slides
The links above will become active on the day before the workshop begins.
Evaluation & Certificate:
Evaluation & Certificate of Attendance
The above link will become active near the close of the first day of the Workshop.
Session Recordings:
Recordings will be linked here as soon as they are available.
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 26, 2024).
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
If you have questions regarding the content of the event or other CDER-specific information, please:
- Visit the CDER SBIA website
- Learn more about CDER SBIA Workshops and Webinars
- Subscribe to the CDER SBIA email updates
- Follow us on LinkedIn