21 CFR 26, Subpart A - Specific Sector Provisions for Pharmaceutical Good Manufacturing Practices
- § 26.1 — Definitions.
- § 26.2 — Purpose.
- § 26.3 — Scope.
- § 26.4 — Product coverage.
- § 26.5 — Length of transition period.
- § 26.6 — Equivalence assessment.
- § 26.7 — Participation in the equivalence assessment and determination.
- § 26.8 — Other transition activities.
- § 26.9 — Equivalence determination.
- § 26.10 — Regulatory authorities not listed as currently equivalent.
- § 26.11 — Start of operational period.
- § 26.12 — Nature of recognition of inspection reports.
- § 26.13 — Transmission of postapproval inspection reports.
- § 26.14 — Transmission of preapproval inspection reports.
- § 26.15 — Monitoring continued equivalence.
- § 26.16 — Suspension.
- § 26.17 — Role and composition of the Joint Sectoral Committee.
- § 26.18 — Regulatory collaboration.
- § 26.19 — Information relating to quality aspects.
- § 26.20 — Alert system.
- § 26.21 — Safeguard clause.
- Appendix A to Subpart A of Part 26 - List of Applicable Laws, Regulations, and Administrative Provisions
- Appendix B to Subpart A of Part 26 - List of Authorities
- Appendix C to Subpart A of Part 26 - Indicative List of Products Covered by Subpart A
- Appendix D to Subpart A of Part 26 - Criteria for Assessing Equivalence for Post- and Preapproval
- Appendix E to Subpart A of Part 26 - Elements To Be Considered in Developing a Two-Way Alert System
Title 21 published on 2012-04-01
no entries appear in the Federal Register after this date.
This is a list of United States Code sections, Statutes at Large, Public Laws, and Presidential Documents, which provide rulemaking authority for this CFR Part.
This list is taken from the Parallel Table of Authorities and Rules provided by GPO [Government Printing Office].
It is not guaranteed to be accurate or up-to-date, though we do refresh the database weekly. More limitations on accuracy are described at the GPO site.
- Appendix A to Subpart A of Part 26 - List of Applicable Laws, Regulations, and Administrative Provisions
- Appendix B to Subpart A of Part 26 - List of Authorities
- Appendix C to Subpart A of Part 26 - Indicative List of Products Covered by Subpart A
- Appendix D to Subpart A of Part 26 - Criteria for Assessing Equivalence for Post- and Preapproval
- Appendix E to Subpart A of Part 26 - Elements To Be Considered in Developing a Two-Way Alert System
