Title 21--Food and Drugs

CHAPTER I--FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES--(Continued)

PART 607--ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS

TEXT PDF607.3 Definitions.
TEXT PDF607.7 Establishment registration and product listing of blood banks and other firms manufacturing human blood and blood products.
TEXT PDF607.20 Who must register and submit a blood product list.
TEXT PDF607.21 Times for establishment registration and blood product listing.
TEXT PDF607.22 How and where to register establishments and list blood products.
TEXT PDF607.25 Information required for establishment registration and blood product listing.
TEXT PDF607.26 Amendments to establishment registration.
TEXT PDF607.30 Updating blood product listing information.
TEXT PDF607.31 Additional blood product listing information.
TEXT PDF607.35 Notification of registrant; blood product establishment registration number and NDC Labeler Code.
TEXT PDF607.37 Inspection of establishment registrations and blood product listings.
TEXT PDF607.39 Misbranding by reference to establishment registration or to registration number.
TEXT PDF607.40 Blood product listing requirements for foreign blood product establishments.
TEXT PDF607.65 Exemptions for blood product establishments.

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