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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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Agenda & Speaker Bios

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Event Agenda

The agenda is still being refined and may be updated over time. The current version is v8, uploaded on November 24, 2024.

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Speaker Biographies

The speaker biographies document provides detailed information for each of the CITC presenters.

Files & Recordings

Download Presentation Slides:

Session Recordings:

Questions & More Information

  • 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.

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    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: