Subpart A - General Provisions

§ 21.1 - Scope.

§ 21.3 - Definitions.

§ 21.10 - Policy concerning records about individuals.

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.

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.

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.

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.

Subpart F - Exemptions

§ 21.60 - Policy.

§ 21.61 - Exempt systems.

§ 21.65 - Access to records in exempt systems.

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.