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Journal Abstract Search
213 related items for PubMed ID: 10291018
1. Impending FDA regulations of healthcare software. First stop: blood banking. Interview by Bill W. Childs. Marrazzo J. US Healthc; 1988 Nov; 5(11):17-8. PubMed ID: 10291018 [No Abstract] [Full Text] [Related]
2. Medical device software regulation: an industry perspective. Simons D. Food Drug Law J; 1997 Nov; 52(2):189-92. PubMed ID: 10557558 [No Abstract] [Full Text] [Related]
3. Patient safety or profit: what incentives are blood shield laws and FDA regulations creating for the tissue banking industry? Williams JL. Indiana Health Law Rev; 2005 Nov; 2(1):295-328. PubMed ID: 17111505 [No Abstract] [Full Text] [Related]
4. Delegations of authority and organization; Ryan White Comprehensive AIDS Resources Emergency Act of 1990--FDA. Final rule. Fed Regist; 1991 Aug 28; 56(167):42527. PubMed ID: 10113840 [Abstract] [Full Text] [Related]
5. Blood and blood components; error and accident reports--Food and Drug Administration. Proposed rule. Fed Regist; 1980 Aug 08; 45(155):52821-4. PubMed ID: 10247831 [Abstract] [Full Text] [Related]
6. FDA final guidance on software validation. Donawa M. Med Device Technol; 2002 Apr 08; 13(3):20-4. PubMed ID: 12030100 [Abstract] [Full Text] [Related]
7. A foot in the door. Interview by Carolyn Dunbar. Simons D. Comput Healthc; 1991 Sep 08; 12(9):57-8. PubMed ID: 10112906 [No Abstract] [Full Text] [Related]
8. Commitment to hospital/physician communication. Interview by Bill W. Childs. Arentowicz F. US Healthc; 1988 Nov 08; 5(11):44, 48, 50. PubMed ID: 10291021 [Abstract] [Full Text] [Related]
10. Software validation and FDA inspections. Young JM. Healthc Inform; 1990 Nov 08; 7(11):34-5. PubMed ID: 10120734 [No Abstract] [Full Text] [Related]
11. Revisions to the requirements applicable to blood, blood components, and source plasma. Final rule. Food and Drug Administration, HHS. Fed Regist; 2001 Aug 06; 66(151):40886-90. PubMed ID: 11732557 [Abstract] [Full Text] [Related]
12. DH&S: providing a broad array of services to healthcare. Interview by Bill W. Childs. Englehart M, Bell R. US Healthc; 1988 Oct 06; 5(10):32-4. PubMed ID: 10291012 [Abstract] [Full Text] [Related]
13. Extended platelet storage makes a welcome difference. Townsend L. MLO Med Lab Obs; 2007 Jun 06; 39(6):40-1. PubMed ID: 17691706 [No Abstract] [Full Text] [Related]
14. HL7: the promise of tomorrow. Interview by Bill W. Childs. Simborg D, Sparks S, Buxton R, Klein J, Van Valkenburgh T, Quinn J, Campbell S, Carney D, Pine S, Glickman M. US Healthc; 1989 Aug 06; 6(8):26, 28, 32. PubMed ID: 10294244 [No Abstract] [Full Text] [Related]
15. 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]
16. The case for the HL7 standard. Simborg DW. Comput Healthc; 1988 Jan 10; 9(1):39-40, 42. PubMed ID: 10285216 [Abstract] [Full Text] [Related]
17. FDA regulation of medical software. Fried BM, Zuckerman JM. J Health Law; 2000 Jan 10; 33(1):129-40. PubMed ID: 10788227 [Abstract] [Full Text] [Related]
19. Data General providing leading-edge solutions. Interview by Bill W. Childs. Raleigh T, Richmond D. US Healthc; 1989 Dec 16; 6(12):37-9. PubMed ID: 10296235 [No Abstract] [Full Text] [Related]
20. Exemption of certain transfusion services and clinical laboratories from registration: Food and Drug Administration. Final rule. Fed Regist; 1980 Dec 30; 45(251 Pt 1):85727-30. PubMed ID: 10298064 [Abstract] [Full Text] [Related] Page: [Next] [New Search]