Code of Federal Regulations (Last Updated: November 8, 2024) |
Title 21 - Food and Drugs |
Chapter I - Food and Drug Administration, Department of Health and Human Services |
SubChapter A - General |
Part 10 - Administrative Practices and Procedures |
Subpart B - General Administrative Procedures |
§ 10.100a - Public calendars.
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(a)
Prospective public calendar of public proceedings . (1) A public calendar will be prepared and made publicly available each week showing, to the extent feasible, for the following 4 weeks, the public meetings, conferences, hearings, advisory committee meetings, seminars, and other public proceedings of FDA, and other significant public events involving FDA, e.g., congressional hearings.(2) A copy of this public calendar will be placed on public display in the following places:
(i) Dockets Management Branch.
(ii) Office of the Associate Commissioner for Public Affairs.
(iii) A central place in each center.
(iv) A central place in each field office.
(v) A central place at the National Center for Toxicological Research.
(b)
Retrospective public calendar of meetings . (1) A public calendar will be prepared and made publicly available each week showing for the previous week meetings with persons outside the executive branch and other significant events involving the representatives of FDA designated under paragraph (b)(3) of this section, but telephone conversations will be included on an optional basis and meetings with the working press, except for “house organs” (i.e., publications of firms that manufacture or distribute regulated products, or industry associations), and with on-site contractors will not be included. Meetings with members of the judiciary, representatives of Congress, or staffs of congressional committees will be included when the meeting relates to a pending court case, administrative hearing, or other regulatory action or decision and involves more than a brief description of the matter.(2) The calendar will include all meetings, conferences, seminars, social events sponsored by the regulated industry, and speeches. The calendar will specify the date and the person and
subject matter involved. When more than one FDA representative is in attendance, only the presiding or head representative will report the meeting on the public calendar. If a large number of persons is involved, the name of each need not be specified. Meetings that would prejudice law enforcement activities (e.g., a meeting with an informant) or invade privacy (e.g., a meeting with a candidate for possible employment in FDA) will not be reported. (3) The following FDA representatives and their deputies are subject to the requirements of paragraphs (b)(1) and (2) of this section:
(i) Commissioner of Food and Drugs.
(ii) Deputy Commissioner.
(iii) Associate Commissioners.
(iv) Executive and Special Assistants to the Commissioner.
(v) [Reserved]
(vi) Director, National Center for Toxicological Research.
(vii) Center Directors.
(viii) Chief Counsel for the Food and Drug Administration, or any representative of that office attending on behalf of the Chief Counsel.
(4) A copy of the public calendar will be placed on public display in the following places:
(i) Dockets Management Branch.
(ii) Office of the Associate Commissioner for Public Affairs.
(iii) A central place in each center.
(iv) A central place in each field office.
(v) A central place at the National Center for Toxicological Research.