21 CFR 58 - GOOD LABORATORY PRACTICE FOR NONCLINICAL LABORATORY STUDIES
- SUBPART A — General Provisions (§§ 58.1 - 58.15)
- SUBPART B — Organization and Personnel (§§ 58.29 - 58.35)
- SUBPART C — Facilities (§§ 58.41 - 58.51)
- SUBPART D — Equipment (§§ 58.61 - 58.63)
- SUBPART E — Testing Facilities Operation (§§ 58.81 - 58.90)
- SUBPART F — Test and Control Articles (§§ 58.105 - 58.113)
- SUBPART G — Protocol for and Conduct of a Nonclinical Laboratory Study (§§ 58.120 - 58.130)
- SUBPART H — I [Reserved]
- SUBPART J — Records and Reports (§§ 58.185 - 58.195)
- SUBPART K — Disqualification of Testing Facilities (§§ 58.200 - 58.219)
Source: 43 FR 60013, Dec. 22, 1978, unless otherwise noted.
Title 21 published on 2011-04-01
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.
