1. Collections
  2. Code of Federal Regulations
  3. Title 21
  4. Chapter I

Subchapter F

Biologics

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    600Biological Products: General601Licensing606Current Good Manufacturing Practice for Blood and Blood Components607Establishment Registration and Product Listing for Manufacturers of Human Blood and Blood Products and Licensed Devices610General Biological Products Standards630Requirements for Blood and Blood Components Intended for Transfusion or for Further Manufacturing Use640Additional Standards for Human Blood and Blood Products660Additional Standards for Diagnostic Substances for Laboratory Tests680Additional Standards for Miscellaneous Products