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21 C.F.R. PART 14--PUBLIC HEARING BEFORE A PUBLIC ADVISORY COMMITTEE

TITLE 21--Food and Drugs

CHAPTER I--FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES

SUBCHAPTER A--GENERAL

PART 14--PUBLIC HEARING BEFORE A PUBLIC ADVISORY COMMITTEE

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

Chairman 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.