21 CFR
Part 607 Establishment Registration and Product Listing for Manufacturers of Human Blood and Blood Products and Licensed Devices
Subpart A - General Provisions
- § 607.1 Scope
- § 607.3 Definitions
- § 607.7 Establishment registration and product listing of blood banks and other firms manufacturing human blood and blood products
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 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 Blood product establishment registration number
- § 607.37 Public disclosure of establishment registration and blood product listing information
- § 607.39 Misbranding by reference to establishment registration, validation of registration, or to registration number