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13. Design considerations for medical device manufacturers. Patel A; Pope J; Neilson M Biomed Instrum Technol; 2012; Suppl():73-5. PubMed ID: 22559781 [No Abstract] [Full Text] [Related]
14. Framework for Alarm Management Process Maturity. Welch J; Rayo M; Kanter B; Bagian T; Jacobs K; Shanawani H; Jaffe R; Conti M; Razzano L Biomed Instrum Technol; 2016; 50(3):165-79. PubMed ID: 27164201 [No Abstract] [Full Text] [Related]
15. Standards in the 21st century. The greening of standardisation. Moore R Med Device Technol; 2001 Apr; 12(3):33. PubMed ID: 11547685 [No Abstract] [Full Text] [Related]
17. From regulation to registration. Safety and performance needs drive industry consensus on voluntary servicing, remarketing controls. Hatem MB Biomed Instrum Technol; 1999; 33(5):393-8. PubMed ID: 10511908 [No Abstract] [Full Text] [Related]
18. Fuzzy logic and medical device design controls. Hess J Med Device Technol; 1996; 7(1):19-22. PubMed ID: 10159865 [TBL] [Abstract][Full Text] [Related]
19. The quality planning conundrum. Donawa ME Med Device Technol; 1999; 10(6):14-6. PubMed ID: 10623345 [TBL] [Abstract][Full Text] [Related]
20. Meeting European and US requirements for design and development documentation, Part I. Donawa ME Med Device Technol; 1996 Nov; 7(9):12-5. PubMed ID: 10163673 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]