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.
132 related articles for article (PubMed ID: 3724590)
1. Establishing a software quality assurance program for microprocessor-based medical equipment. Fries RC; Heide PW Med Instrum; 1986; 20(3):156-61. PubMed ID: 3724590 [No Abstract] [Full Text] [Related]
2. Regulation of medical software by the Food and Drug Administration. Jorgens J; Schneider RH Softw Healthc; 1985; 3(2):27-9. PubMed ID: 10278374 [No Abstract] [Full Text] [Related]
3. FDA & Y2K. Preparing for the new millennium. Lewis C FDA Consum; 1999; 33(6):6-11. PubMed ID: 10628310 [No Abstract] [Full Text] [Related]
4. US quality system requirements for software validation. Donawa ME Med Device Technol; 1998 Mar; 9(2):17-20. PubMed ID: 10186973 [TBL] [Abstract][Full Text] [Related]
5. Medical devices: assuring quality control through federal agencies. Harken DE Bull Am Coll Surg; 1980 Jun; 65(6):15-7. PubMed ID: 10297804 [No Abstract] [Full Text] [Related]
6. Validation of computerized membrane integrity test systems. Wolber P; Beech D; McAllister M J Parenter Sci Technol; 1988; 42(4):106-10. PubMed ID: 3183863 [No Abstract] [Full Text] [Related]
7. Medical device regs: are they doing the job? Higher cost, even delayed availability, are a possibility. Smith GF AORN J; 1981 Apr; 33(5):958-60. PubMed ID: 6908514 [No Abstract] [Full Text] [Related]
8. User problems and medical device recalls. Mosenkis R Med Instrum; 1986; 20(4):226. PubMed ID: 3762454 [No Abstract] [Full Text] [Related]
9. Micromatrix. Computers, medicine, and quality control. Grundner TM Health Matrix; 1984; 2(1):57. PubMed ID: 10278285 [TBL] [Abstract][Full Text] [Related]
11. Medical device surveillance world-wide. Badea C; Kolitsi Z; Pallikarakis N; Papapanagiotou A Stud Health Technol Inform; 1996; 28():157-74. PubMed ID: 10184634 [No Abstract] [Full Text] [Related]
12. FDA's Quality System Inspection Technique in Ireland. Higgins S Med Device Technol; 2001; 12(1):40-1. PubMed ID: 11317865 [No Abstract] [Full Text] [Related]
13. Vioxx, radiology, and the Food and Drug Administration. Pentecost MJ J Am Coll Radiol; 2005 May; 2(5):394-7. PubMed ID: 17411841 [No Abstract] [Full Text] [Related]
14. Medical device regs: are they doing the job? FDA and industry share common goal of device safety. McDonnell EJ AORN J; 1981 Apr; 33(5):949-54. PubMed ID: 6908513 [No Abstract] [Full Text] [Related]
15. Medical device regulation in the United States and the European Union: a comparative study. Chai JY Food Drug Law J; 2000; 55(1):57-80. PubMed ID: 12296349 [No Abstract] [Full Text] [Related]
16. FDA software policy and regulation of medical device software. Crumpler ES; Rudolph H Food Drug Law J; 1997; 52(4):511-6. PubMed ID: 10346676 [No Abstract] [Full Text] [Related]
17. Endotoxin testing of medical devices with LAL: FDA requirements. Ross VC; Bruch CW Prog Clin Biol Res; 1982; 93():39-48. PubMed ID: 6750646 [No Abstract] [Full Text] [Related]
19. Differing definitions of manufacturer. Donawa ME Med Device Technol; 1998; 9(6):14-7. PubMed ID: 10182120 [TBL] [Abstract][Full Text] [Related]
20. Complying with US and European complaint handling requirements. Donawa ME Med Device Technol; 1997 Sep; 8(7):12-5. PubMed ID: 10174197 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]