TITLE 21--FOOD AND DRUGS CHAPTER I--FOOD AND DRUG ADMINISTRATION DEPARTMENT OF HEALTH AND HUMAN SERVICES
SUBCHAPTER F - BIOLOGICS
Subpart A - General Provisions
§ 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.
Subpart B - Procedures for Domestic Blood Product Establishments
§ 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.
Subpart C - Procedures for Foreign Blood Product Establishments
§ 607.40 - Establishment registration and blood product listing requirements for foreign blood product establishments.
Subpart D - Exemptions
§ 607.65 - Exemptions for blood product establishments.
Subpart E - Establishment Registration and Product Listing Of Licensed Devices
§ 607.80 - Applicability of part 607 to licensed devices.
|
Authority: 21 U.S.C. 321, 331, 351, 352, 355, 360, 371, 374, 381, 393; 42 U.S.C. 262, 264, 271.
Source: 40 FR 52788, Nov. 12, 1975, unless otherwise noted.
|