Title 21, Part 607 — Establishment Registration and Product Listing for Manufacturers of Human Blood and Blood Products and Licensed Devices
16 sections
Section 607.1
Scope.
Section 607.3
Definitions.
Section 607.7
Establishment registration and product listing of blood banks and other firms manufacturing human blood and blood products.
Section 607.20
Who must register and submit a blood product list.
Section 607.21
Times for establishment registration and blood product listing.
Section 607.22
How to register establishments and list blood products.
Section 607.25
Information required for establishment registration and blood product listing.
Section 607.26
Amendments to establishment registration.
Section 607.30
Updating blood product listing information.
Section 607.31
Additional blood product listing information.
Section 607.35
Blood product establishment registration number.
Section 607.37
Public disclosure of establishment registration and blood product listing information.
Section 607.39
Misbranding by reference to establishment registration, validation of registration, or to registration number.
Section 607.40
Establishment registration and blood product listing requirements for foreign blood product establishments.
Section 607.65
Exemptions for blood product establishments.
Section 607.80
Applicability of part 607 to licensed devices.