These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
145 related articles for article (PubMed ID: 10116935)
1. The laboratory information system as a medical device: inspection and accreditation issues. Aller RD Clin Lab Manage Rev; 1992; 6(1):58-64. PubMed ID: 10116935 [TBL] [Abstract][Full Text] [Related]
2. Regulation of clinical laboratory information systems after the 1990 amendments to the Food and Drug Act. Brannigan VM Clin Lab Manage Rev; 1992; 6(1):49-50, 52, 54-7. PubMed ID: 10116934 [TBL] [Abstract][Full Text] [Related]
3. The quest for quality blood banking program in the new millennium the American way. Kim DU Int J Hematol; 2002 Aug; 76 Suppl 2():258-62. PubMed ID: 12430934 [TBL] [Abstract][Full Text] [Related]
4. Software regression testing and quality assurance. Weilert M Am J Clin Pathol; 1996 Apr; 105(4 Suppl 1):S10-6. PubMed ID: 8607456 [TBL] [Abstract][Full Text] [Related]
5. Required steps for the validation of a Laboratory Information Management System. Turner E; Bolton J Qual Assur; 2001; 9(3-4):217-24. PubMed ID: 12553085 [TBL] [Abstract][Full Text] [Related]
6. Laboratory information system test environment: validate upgrades, prevent disasters, and assist training. Ashwood ER; Labart PL Clin Lab Manage Rev; 1992; 6(1):66-8, 70-1. PubMed ID: 10116936 [TBL] [Abstract][Full Text] [Related]
7. Voluntary accreditation of cellular therapies: Foundation for the Accreditation of Cellular Therapy (FACT). Warkentin PI; Cytotherapy; 2003; 5(4):299-305. PubMed ID: 12944235 [TBL] [Abstract][Full Text] [Related]
9. The Safe Medical Devices Act of 1990: are hospitals ready to deal with the FDA? Loob WH J Clin Eng; 1991; 16(1):35-48. PubMed ID: 10109830 [TBL] [Abstract][Full Text] [Related]
11. Computer validation in toxicology: historical review for FDA and EPA good laboratory practice. Brodish DL Qual Assur; 1998; 6(4):185-99. PubMed ID: 10647148 [TBL] [Abstract][Full Text] [Related]
12. Approval of the Commission on Office Laboratory Accreditation--HCFA. Notice. Fed Regist; 1993 Dec; 58(245):68148-51. PubMed ID: 10131227 [TBL] [Abstract][Full Text] [Related]
13. Medical devices; device tracking--FDA. Final rule; suspension of effective date; notification of status under the Safe Medical Devices Act; technical amendments. Fed Regist; 1993 Aug; 58(156):43442-51. PubMed ID: 10127886 [TBL] [Abstract][Full Text] [Related]
14. Letter to manufacturers of blood establishment computer software products--FDA. Notice. Fed Regist; 1994 Aug; 59(168):44991-2. PubMed ID: 10136917 [TBL] [Abstract][Full Text] [Related]
15. Taking the risk out of laboratory information systems. Winsten DI Clin Lab Manage Rev; 1992; 6(1):39-40, 42-4, 46-8. PubMed ID: 10116933 [TBL] [Abstract][Full Text] [Related]
16. What do the accreditation organizations expect? American Association of Blood Banks. Otter J; Cooper ES Arch Pathol Lab Med; 1999 Jun; 123(6):468-71. PubMed ID: 10383794 [TBL] [Abstract][Full Text] [Related]
17. LIMS user acceptance testing. Klein CS Qual Assur; 2003; 10(2):91-106. PubMed ID: 14660299 [TBL] [Abstract][Full Text] [Related]
18. Medical device software regulation: an industry perspective. Simons D Food Drug Law J; 1997; 52(2):189-92. PubMed ID: 10557558 [No Abstract] [Full Text] [Related]
19. Point of care testing: regulation and accreditation. Carlson DA Clin Lab Sci; 1996; 9(5):298-302; quiz 303-4. PubMed ID: 10163657 [TBL] [Abstract][Full Text] [Related]