Federal (United States) · Regulations
Subpart B — Procedures for Domestic Blood Product Establishments
10 sections
10 sections
- 21 C.F.R. § 607.20Who must register and submit a blood product list.
- 21 C.F.R. § 607.21Times for establishment registration and blood product listing.
- 21 C.F.R. § 607.22How to register establishments and list blood products.
- 21 C.F.R. § 607.25Information required for establishment registration and blood product listing.
- 21 C.F.R. § 607.26Amendments to establishment registration.
- 21 C.F.R. § 607.30Updating blood product listing information.
- 21 C.F.R. § 607.31Additional blood product listing information.
- 21 C.F.R. § 607.35Blood product establishment registration number.
- 21 C.F.R. § 607.37Public disclosure of establishment registration and blood product listing information.
- 21 C.F.R. § 607.39Misbranding by reference to establishment registration, validation of registration, or to registration number.