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# FDA Plans Workshop on Clinical Trial Requirements
- URL: https://www.fdaweb.com/fda-plans-workshop-on-clinical-trial-requirements/
- Published: 2016-02-16T12:00:00.000Z
- Updated: 2026-09-15T02:36:02.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5134782

*Federal Register* Notice: FDA will hold a public workshop 3/9-10 entitled “Educational Conference Co-Sponsored with the Society of Clinical Research Associates (SOCRA).” The workshop on FDA’s clinical trial requirements is designed to aid the Clinical Research Professional’s understanding of the mission, responsibilities, and authority of FDA and to facilitate interaction with FDA representatives. The program will focus on the relationships among FDA, clinical trial staff, investigators, and institutional review boards (IRBs). Individual FDA representatives will discuss the informed consent process and informed consent documents; regulations relating to drugs, devices, and biologics; as well as inspections of clinical investigators, of IRBs, and of research sponsors. The workshop will be held on both days from 8 a.m. to 5 p.m. at the Holiday Inn San Diego Bayside, 4875 North Harbor Dr., San Diego, CA. Contact **Jane Kreis** (510) 287-2708 or Society of Clinical Research Associates (800) 762-7292 or (215) 822-8644\. To view this notice, click [here](https://www.gpo.gov/fdsys/pkg/FR-2016-02-16/pdf/2016-02965.pdf?ref=fdaweb.com).