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U.S. Code of Federal Regula...
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Title 21-Food and Drugs
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CHAPTER I—FOOD AND DRUG ADM...
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PART 607—ESTABLISHMENT REGISTRATION AND PRODUCT...
PART 607—ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS AND LICENSED DEVICES
§ 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.