Part 607 — Establishment Registration and Product Listing for Manufacturers of Human Blood and Blood Products and Licensed Devices
Subpart A — General Provisions
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.