part_subject: "PUBLIC HEARING BEFORE A PUBLIC ADVISORY COMMITTEE"
subpart_code: "B"
subpart_subject: "Meeting Procedures"
section_number: "14.33"
section_subject: "Compilation of materials for members of an advisory committee."
cfr_reference: "21 CFR 14.33"
title_name: "Title 21"
title_subject: "Food and Drugs"
parts_covered: "Parts 1 to 99"
revised_date: "Revised as of April 1, 2019"
publication_date: "As of April 1, 2019"
contains_description: "Containing a codification of documents of general applicability and future effect"
publication_info: "Published by the Office of the Federal Register National Archives and Records Administration as a Special Edition of the Federal Register"
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The Commissioner shall prepare and provide to all committee members a compilation of materials bearing upon members' duties and responsibilities, including—
(a)All applicable conflict of interest laws and regulations and a summary of their principal provisions;
(b)All applicable laws and regulations relating to trade secrets and confidential commercial or financial information that may not be disclosed publicly and a summary of their principal provisions;
(c)All applicable laws, regulations, and guidance documents relating to the subject matter covered by the advisory committee and a summary of their principal provisions;
(d)All applicable laws, regulations, including the regulations in part 20 of this chapter, advisory committee charters, Federal Register notices, curricula vitae, rules adopted by the advisory committee, and other material relating to the formation, composition, and operation of the advisory committee, and a summary of their principal provisions;
(e)Instructions on whom to contact when questions arise; and
(f)Other material relating to FDA and the subject matter covered by the committee which may facilitate the work of the committee.