About GPO   |   Newsroom/Media   |   Congressional Relations   |   Inspector General   |   Careers   |   Contact   |   askGPO   |   Help  
 
Home   |   Customers   |   Vendors   |   Libraries  

The Electronic Code of Federal Regulations (e-CFR) is a regularly updated, unofficial editorial compilation of CFR material and Federal Register amendments produced by the National Archives and Records Administration's Office of the Federal Register (OFR) and the Government Printing Office.

Parallel Table of Authorities and Rules for the Code of Federal Regulations and the United States Code
Text | PDF

Find, review, and submit comments on Federal rules that are open for comment and published in the Federal Register using Regulations.gov.

Purchase individual CFR titles from the U.S. Government Online Bookstore.

Find issues of the CFR (including issues prior to 1996) at a local Federal depository library.

[2]
 
 

Electronic Code of Federal Regulations

blue pill

e-CFR Data is current as of November 21, 2014

Title 21Chapter ISubchapter APart 21


TITLE 21—Food and Drugs

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

SUBCHAPTER A—GENERAL

PART 21—PROTECTION OF PRIVACY

rule

Subpart A—GENERAL PROVISIONS

§21.1
Scope.
§21.3
Definitions.
§21.10
Policy concerning records about individuals.
rule

Subpart B—FOOD AND DRUG ADMINISTRATION PRIVACY ACT RECORD SYSTEMS

§21.20
Procedures for notice of Food and Drug Administration Privacy Act Record Systems.
§21.21
Changes in systems and new systems.
rule

Subpart C—REQUIREMENTS FOR SPECIFIC CATEGORIES OF RECORDS

§21.30
Records of contractors.
§21.31
Records stored by the National Archives and Records Administration.
§21.32
Personnel records.
§21.33
Medical records.
rule

Subpart D—PROCEDURES FOR NOTIFICATION OF AND ACCESS TO RECORDS IN PRIVACY ACT RECORD SYSTEMS

§21.40
Procedures for submitting requests for notification and access.
§21.41
Processing of requests.
§21.42
Responses to requests.
§21.43
Access to requested records.
§21.44
Verification of identity.
§21.45
Fees.
rule

Subpart E—PROCEDURES FOR REQUESTS FOR AMENDMENT OF RECORDS

§21.50
Procedures for submitting requests for amendment of records.
§21.51
Responses to requests for amendment of records.
§21.52
Administrative appeals of refusals to amend records.
§21.53
Notation and disclosure of disputed records.
§21.54
Amended or disputed records received from other agencies.
rule

Subpart F—EXEMPTIONS

§21.60
Policy.
§21.61
Exempt systems.
§21.65
Access to records in exempt systems.
rule

Subpart G—DISCLOSURE OF RECORDS IN PRIVACY ACT RECORD SYSTEMS TO PERSONS OTHER THAN THE SUBJECT INDIVIDUAL

§21.70
Disclosure and intra-agency use of records in Privacy Act Record Systems; no accounting required.
§21.71
Disclosure of records in Privacy Act Record Systems; accounting required.
§21.72
Individual consent to disclosure of records to other persons.
§21.73
Accuracy, completeness, timeliness, and relevance of records disclosed from Privacy Act Record Systems.
§21.74
Providing notice that a record is disputed.
§21.75
Rights of legal guardians.


For questions or comments regarding e-CFR editorial content, features, or design, email ecfr@nara.gov.
For questions concerning e-CFR programming and delivery issues, email webteam@gpo.gov.