172 related articles for article (PubMed ID: 10164095)
21. [Safety of high risk in vitro diagnostic medical devices : international and national measures].
Halbauer J; Siekmeier R; Funk M
Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz; 2009 Jun; 52(6):610-8. PubMed ID: 19421725
[TBL] [Abstract][Full Text] [Related]
22. Clinical evaluations clinical investigations under the amended Medical Device Directive.
Dannhorn DR; Schwabedissen H
Med Device Technol; 2008 Sep; 19(5):16-8, 20. PubMed ID: 18947145
[TBL] [Abstract][Full Text] [Related]
23. Serious adverse event reporting in a medical device information system.
Pecoraro F; Luzi D
Stud Health Technol Inform; 2011; 169():834-8. PubMed ID: 21893864
[TBL] [Abstract][Full Text] [Related]
24. FDA modernization act of 1997: guidance on medical device tracking; availability--FDA. Notice.
Fed Regist; 1998 Mar; 63(42):10640-1. PubMed ID: 10177505
[TBL] [Abstract][Full Text] [Related]
25. Requirements specification for a harmonized medical device vigilance information exchange system.
Vassilacopoulos G
Stud Health Technol Inform; 1996; 28():39-44. PubMed ID: 10172829
[TBL] [Abstract][Full Text] [Related]
26. European requirements for product returns.
Donawa M
Med Device Technol; 2005 Nov; 16(9):28-31. PubMed ID: 16438446
[TBL] [Abstract][Full Text] [Related]
27. The EUROMEDIES concerted action outcomes.
Vassilacopoulos G; Pangalos G; Doukidis G; Pramataris K; Pallikarakis N
Stud Health Technol Inform; 1996; 28():175-217. PubMed ID: 10172835
[No Abstract] [Full Text] [Related]
28. [Medical Devices Law for anesthesiologists].
Regner M
Anaesthesist; 2015 Sep; 64(9):711-21; quiz 722-3. PubMed ID: 26349426
[TBL] [Abstract][Full Text] [Related]
29. [Medical devices and patient safety from the clinicians' view].
Mellert F; Mallek D
Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz; 2009 Jun; 52(6):584-8. PubMed ID: 19436959
[TBL] [Abstract][Full Text] [Related]
30. EU and US clinical investigation adverse event reporting.
Crowley G
Med Device Technol; 2004 Jun; 15(5):30-2. PubMed ID: 15285486
[TBL] [Abstract][Full Text] [Related]
31. German law: the differences.
Müller-Lierheim WG
Med Device Technol; 1997 Nov; 8(9):38-40. PubMed ID: 10174630
[TBL] [Abstract][Full Text] [Related]
32. [Guidelines on medical devices vigilance system of European Commission & its enlightenment to China].
Tang H; Linghu CL; Yang Y
Zhongguo Yi Liao Qi Xie Za Zhi; 2009 Mar; 33(3):212-4. PubMed ID: 19771900
[TBL] [Abstract][Full Text] [Related]
33. US and European postmarket clinical data requirements.
Donawa M
Med Device Technol; 2005 Mar; 16(2):19-21. PubMed ID: 15828495
[TBL] [Abstract][Full Text] [Related]
34. Medical devices on trial, Part I.
Wright D
Med Device Technol; 2002 Dec; 13(10):35-8. PubMed ID: 12575529
[TBL] [Abstract][Full Text] [Related]
35. [The medical devices vigilance system].
Meria P; Pariente JL; Conort P
Prog Urol; 2005 Nov; 15(5):1000-4. PubMed ID: 16475665
[No Abstract] [Full Text] [Related]
36. User reporting of medical device related incidents.
Sievänen H
Med Device Technol; 2003 May; 14(4):26-9. PubMed ID: 12774575
[TBL] [Abstract][Full Text] [Related]
37. [Medical devices vigilance].
Crickx B
Ann Dermatol Venereol; 2008 Jan; 135(1 Pt 2):1S70-2. PubMed ID: 18442667
[TBL] [Abstract][Full Text] [Related]
38. [Importance of the Therapeutic Products Act for the ENT practitioner].
Kaiser R; Ininger G; Stosslein E
HNO; 2003 Jun; 51(6):513-24; quiz 525-6. PubMed ID: 12858855
[TBL] [Abstract][Full Text] [Related]
39. European Animal Tissue Directive.
Donawa M
Med Device Technol; 2004; 15(1):28-31. PubMed ID: 14994636
[TBL] [Abstract][Full Text] [Related]
40. [Information on the policies of the Medical Devices Safety Act].
Wetzel D; von Mallek D
Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz; 2009 Jun; 52(6):577-8. PubMed ID: 19407937
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]