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Title 21
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Part 607
FEDERAL · 21 CFR
Part 607 — Establishment Registration and Product Listing for Manufacturers of Human Blood and Blood Products and Licensed Devices
16 sections · Title 21: Food and Drugs
§ 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.
§ 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.
§ 607.40
Establishment registration and blood product listing requirements for foreign blood product establishments.
§ 607.65
Exemptions for blood product establishments.
§ 607.80
Applicability of part 607 to licensed devices.