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Title 21

Displaying title 21, up to date as of 9/10/2026. Title 21 was last amended 9/10/2026.
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  1. Title 21 —Food and Drugs
  2. Chapter I —Food and Drug Administration, Department of Health and Human Services
  3. Subchapter A —General
  4. Part 14   View Full Text
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Title 21Food and DrugsPart / Section
Chapter IFood and Drug Administration, Department of Health and Human Services1 – 1299
Subchapter AGeneral1 – 99
Part 14Public Hearing Before a Public Advisory Committee14.1 – 14.174
Subpart AGeneral Provisions14.1 – 14.15
§ 14.1Scope.
§ 14.5Purpose of proceedings before an advisory committee.
§ 14.7Administrative remedies.
§ 14.10Applicability to Congress.
§ 14.15Committees working under a contract with FDA.
Subpart BMeeting Procedures14.20 – 14.39
Subpart CEstablishment of Advisory Committees14.40 – 14.55
§ 14.40Establishment and renewal of advisory committees.
§ 14.55Termination of advisory committees.
Subpart DRecords of Meetings and Hearings Before Advisory Committees14.60 – 14.75
Subpart EMembers of Advisory Committees14.80 – 14.95
Subpart FStanding Advisory Committees14.100
§ 14.100List of standing advisory committees.
Subpart GTechnical Electronic Products Radiation Safety Standards Committee14.120 – 14.130
Subpart HColor Additive Advisory Committees14.140 – 14.155
Subpart IAdvisory Committees for Human Prescription Drugs14.160 – 14.174
§ 14.160Establishment of standing technical advisory committees for human prescription drugs.
§ 14.171Utilization of an advisory committee on the initiative of FDA.
§ 14.172Utilization of an advisory committee at the request of an interested person.
§ 14.174Advice and recommendations in writing.
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