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2. Revisions to the requirements applicable to blood, blood components, and source plasma. Department of Health and Human Services (HHS), Public Health Service (PHS), Food and Drug Administration (FDA). Direct final rule. Fed Regist; 1999 Aug 19; 64(160):45366-74. PubMed ID: 10558597 [Abstract] [Full Text] [Related]
3. Revisions to the requirements applicable to blood, blood components, and source plasma; confirmation in part and technical amendment. Food and Drug Administration, HHS. Direct final rule; confirmation in part and technical amendment. Fed Regist; 2001 Jan 10; 66(7):1834-7. PubMed ID: 11503754 [Abstract] [Full Text] [Related]
4. Revisions to the requirements applicable to blood, blood components and source plasma. Direct final rule. Food and Drug Administration, HHS. Fed Regist; 2007 Aug 16; 72(158):45883-88. PubMed ID: 17847577 [Abstract] [Full Text] [Related]
7. Revision of requirements applicable to albumin (human), plasma protein fraction (human), and immune globulin (human). Food and Drug Administration, HHS. Direct final rule. Fed Regist; 1999 May 14; 64(93):26282-7. PubMed ID: 10558530 [Abstract] [Full Text] [Related]
8. Revision of requirements applicable to albumin (human), plasma protein fraction (human), and immune globulin (human); companion document to direct final rule. Food and Drug Administration, HHS. Proposed rule. Fed Regist; 1999 May 14; 64(93):26344-8. PubMed ID: 10558531 [Abstract] [Full Text] [Related]
9. Current good manufacturing practices for blood and blood components: notification of consignees receiving blood and blood components at increased risk for transmitting HIV infection--FDA. Final rule. Fed Regist; 1996 Sep 09; 61(175):47413-23. PubMed ID: 10160337 [Abstract] [Full Text] [Related]
10. Revision to requirements for licensed Anti-Human Globulin and Blood Grouping Reagents. Food and Drug Administration, HHS. Direct final rule. Fed Regist; 2000 Dec 12; 65(239):77497-9. PubMed ID: 11503726 [Abstract] [Full Text] [Related]