Good Clinical Practice (GCP) eRegs & Guides - For Your Reference Book 9

PART 600 BIOLOGICAL PRODUCTS: GENERAL 

PART 601 LICENSING 

PART 606 CURRENT GOOD MANUFACTURING PRACTICE FOR BLOOD AND BLOOD COMPONENTS 

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

PART 610 GENERAL BIOLOGICAL PRODUCTS STANDARDS 

PART 630 GENERAL REQUIREMENTS FOR BLOOD, BLOOD COMPONENTS, AND BLOOD DERIVATIVES 

PART 640 ADDITIONAL STANDARDS FOR HUMAN BLOOD AND BLOOD PRODUCTS 

PART 660 ADDITIONAL STANDARDS FOR DIAGNOSTIC SUBSTANCES FOR LABORATORY TESTS 

PART 680 ADDITIONAL STANDARDS FOR MISCELLANEOUS PRODUCTS 

PART 1270 HUMAN TISSUE INTENDED FOR TRANSPLANTATION 

PART 1271 HUMAN CELLS, TISSUES, AND CELLULAR AND TISSUE-BASED PRODUCTS 

Guidance for Industry: Eligibility Determination for Donors of Human Cells, Tissues, and Cellular and Tissue-Based Products