FDA 21 CFR Part 600 to 680 Guidelines for Biologics

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FDA 21 CFR PART 600 TO 680 SUBCHAPTER F — BIOLOGICS

Click on the titles below for complete guidelines


21 CFR Part 600 Biological Products: General

21 CFR Part 601 Licensing

21 CFR Part 606 Current Good Manufacturing Practice For Blood And Blood Components

21 CFR Part 607 Establishment Registration And Product Listing For Manufacturers Of Human Blood And Blood Products And Licensed Devices

21 CFR Part 610 General Biological Products Standards

21 CFR Part 630 Requirements For Blood And Blood Components Intended For Transfusion Or For Further Manufacturing Use

21 CFR Part 640 Additional Standards For Human Blood And Blood Products

21 CFR Part 660 Additional Standards For Diagnostic Substances For Laboratory Tests

21 CFR Part 680 Additional Standards For Miscellaneous Products


FDA 21 CFR Part 600 to 680 Guidelines for Biologics:


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