21 CFR Part 26 - MUTUAL RECOGNITION OF PHARMACEUTICAL GOOD MANUFACTURING PRACTICE REPORTS, MEDICAL DEVICE QUALITY SYSTEM AUDIT REPORTS, AND CERTAIN MEDICAL DEVICE PRODUCT EVALUATION REPORTS: UNITED STATES AND THE EUROPEAN COMMUNITY
- § 26.0 — General.
- SUBPART A — Specific Sector Provisions for Pharmaceutical Good Manufacturing Practices (§§ 26.1 - 26.21)
- SUBPART B — Specific Sector Provisions for Medical Devices (§§ 26.31 - 26.50)
- SUBPART C — “Framework” Provisions (§§ 26.60 - 26.81)
Authority:
Source:
63 FR 60141, Nov. 6, 1998, unless otherwise noted.
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.
