21 CFR 607, Subpart B - Procedures for Domestic Blood Product Establishments
- § 607.20 — Who must register and submit a blood product list.
- § 607.21 — Times for establishment registration and blood product listing.
- § 607.22 — How and where to register establishments and list blood products.
- § 607.25 — Information required for establishment registration and blood product listing.
- § 607.26 — Amendments to establishment registration.
- § 607.30 — Updating blood product listing information.
- § 607.31 — Additional blood product listing information.
- § 607.35 — Notification of registrant; blood product establishment registration number and NDC Labeler Code.
- § 607.37 — Inspection of establishment registrations and blood product listings.
- § 607.39 — Misbranding by reference to establishment registration or to registration number.
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.
