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 ProductsRequests bya licensed manufacturer to submit reports attimes other than those stated should be made as a request for a waiver under 600.90. [59 FR 54042, Oct . 27, 1994, as amended at 64 FR 56449, Oct. 20, 1999; 70 FR 14983, Mar.
|Title||:||Good Clinical Practice eRegs & Guides - For Your Reference Book 9: Regulations & Guidance on Biologics, Blood Products, and Good Tissue Practice|
|Author||:||eRegs & Guides, Biopharma Advantage Consulting L.LC.|
|Publisher||:||eregs & guides -|