21 CFR Part 606 - CURRENT GOOD MANUFACTURING PRACTICE FOR BLOOD AND BLOOD COMPONENTS
- SUBPART A — General Provisions (§§ 606.3 - 606.3)
- SUBPART B — Organization and Personnel (§§ 606.20 - 606.20)
- SUBPART C — Plant and Facilities (§§ 606.40 - 606.40)
- SUBPART D — Equipment (§§ 606.60 - 606.65)
- SUBPART E — [Reserved]
- SUBPART F — Production and Process Controls (§§ 606.100 - 606.110)
- SUBPART G — Finished Product Control (§§ 606.120 - 606.122)
- SUBPART H — Laboratory Controls (§§ 606.140 - 606.151)
- SUBPART I — Records and Reports (§§ 606.160 - 606.171)
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.
