Statutes, codes, and regulations
Code of Federal Regulations
Title 21 - FOOD AND DRUGSChapter I - FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICESSubchapter F - BIOLOGICSPart 607 - ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS AND LICENSED DEVICES
Subpart A - GENERAL PROVISIONS
Section 607.7 - Establishment registration and product listing of blood banks and other firms manufacturing human blood and blood products

21 C.F.R. § 607.7

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Current through March 31, 2024
Section 607.7 - Establishment registration and product listing of blood banks and other firms manufacturing human blood and blood products

All owners or operators of establishments that engage in the manufacturing of blood products are required to register, pursuant to section 510 of the Federal Food, Drug, and Cosmetic Act. Registration and listing of blood products must comply with this part. Registration does not permit any blood bank or similar establishment to ship blood products in interstate commerce.

21 C.F.R. §607.7

81 FR 60222, Aug. 31, 2016