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October 01 , 2018

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

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Overview

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

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