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Title 21 - Title 21

Part 607 - ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS AND LICENSED DEVICES

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Details about Part 607

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BIOLOGICS - ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS AND LICENSED DEVICES

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16 sections

§607.1 - Scope.

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§607.20 - Who must register and submit a blood product list.

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§607.21 - Times for establishment registration and blood product listing.

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§607.22 - How to register establishments and list blood products.

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§607.25 - Information required for establishment registration and blood product listing.

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§607.26 - Amendments to establishment registration.

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§607.3 - Definitions.

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§607.30 - Updating blood product listing information.

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§607.31 - Additional blood product listing information.

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§607.35 - Blood product establishment registration number.

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§607.37 - Public disclosure of establishment registration and blood product listing information.

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§607.39 - Misbranding by reference to establishment registration, validation of registration, or to registration number.

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§607.40 - Establishment registration and blood product listing requirements for foreign blood product establishments.

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§607.65 - Exemptions for blood product establishments.

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§607.7 - Establishment registration and product listing of blood banks and other firms manufacturing human blood and blood products.

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§607.80 - Applicability of part 607 to licensed devices.

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