21 CFR Part 14
PART 14—PUBLIC HEARING BEFORE A PUBLIC ADVISORY COMMITTEE
- PART 14—PUBLIC HEARING BEFORE A PUBLIC ADVISORY COMMITTEE
- Chapter I—Food and Drug Administration, Department of Health and Human Services › Subchapter A—General
- Subpart A—General Provisions
- § 14.1 Scope.
- § 14.5 Purpose of proceedings before an advisory committee.
- § 14.7 Administrative remedies.
- § 14.10 Applicability to Congress.
- § 14.15 Committees working under a contract with FDA.
- Subpart B—Meeting Procedures
- § 14.20 Notice of hearing before an advisory committee.
- § 14.22 Meetings of an advisory committee.
- § 14.25 Portions of advisory committee meetings.
- § 14.27 Determination to close portions of advisory committee meetings.
- § 14.29 Conduct of a hearing before an advisory committee.
- § 14.30 Chairperson of an advisory committee.
- § 14.31 Consultation by an advisory committee with other persons.
- § 14.33 Compilation of materials for members of an advisory committee.
- § 14.35 Written submissions to an advisory committee.
- § 14.39 Additional rules for a particular advisory committee.
- Subpart C—Establishment of Advisory Committees
- § 14.40 Establishment and renewal of advisory committees.
- § 14.55 Termination of advisory committees.
- Subpart D—Records of Meetings and Hearings Before Advisory Committees
- § 14.60 Minutes and reports of advisory committee meetings.
- § 14.61 Transcripts of advisory committee meetings.
- § 14.65 Public inquiries and requests for advisory committee records.
- § 14.70 Administrative record of a public hearing before an advisory committee.
- § 14.75 Examination of administrative record and other advisory committee records.
- Subpart E—Members of Advisory Committees
- § 14.80 Qualifications for members of standing policy and technical advisory committees.
- § 14.82 Nominations of voting members of standing advisory committees.
- § 14.84 Nominations and selection of nonvoting members of standing technical advisory committees.
- § 14.86 Rights and responsibilities of nonvoting members of advisory committees.
- § 14.90 Ad hoc advisory committee members.
- § 14.95 Compensation of advisory committee members.
- Subpart F—Standing Advisory Committees
- § 14.100 List of standing advisory committees.
- Subpart G—Technical Electronic Products Radiation Safety Standards Committee
- § 14.120 Establishment of the Technical Electronic Product Radiation Safety Standards Committee (TEPRSSC).
- § 14.122 Functions of TEPRSSC.
- § 14.125 Procedures of TEPRSSC.
- § 14.127 Membership of TEPRSSC.
- § 14.130 Conduct of TEPRSSC meeting; availability of TEPRSSC records.
- Subpart H—Color Additive Advisory Committees
- § 14.140 Establishment of a color additive advisory committee.
- § 14.142 Functions of a color additive advisory committee.
- § 14.145 Procedures of a color additive advisory committee.
- § 14.147 Membership of a color additive advisory committee.
- § 14.155 Fees and compensation pertaining to a color additive advisory committee.
- Subpart I—Advisory Committees for Human Prescription Drugs
- § 14.160 Establishment of standing technical advisory committees for human prescription drugs.
- § 14.171 Utilization of an advisory committee on the initiative of FDA.
- § 14.172 Utilization of an advisory committee at the request of an interested person.
- § 14.174 Advice and recommendations in writing.
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