163 related articles for article (PubMed ID: 19771900)
1. [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]
2. Implementing new European vigilance procedures.
Donawa M
Med Device Technol; 2007; 18(7):34, 36-7. PubMed ID: 18075133
[TBL] [Abstract][Full Text] [Related]
3. Medical devices vigilance: the European approach.
Freeman MF
Stud Health Technol Inform; 1996; 28():13-6. PubMed ID: 10172826
[TBL] [Abstract][Full Text] [Related]
4. Review of the Medical Device Directive.
Donawa M
Med Device Technol; 2003 Mar; 14(2):20-3. PubMed ID: 12698694
[TBL] [Abstract][Full Text] [Related]
5. Update on the European database.
Donawa M
Med Device Technol; 2001 Oct; 12(8):21-4. PubMed ID: 12938545
[TBL] [Abstract][Full Text] [Related]
6. User reporting systems.
Donawa ME
Med Device Technol; 1997 Dec; 8(10):10-2. PubMed ID: 10176361
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Proposed amendments to the medical devices Directives.
Donawa M
Med Device Technol; 2006; 17(1):22-5. PubMed ID: 16483107
[TBL] [Abstract][Full Text] [Related]
9. European requirements for product returns.
Donawa M
Med Device Technol; 2005 Nov; 16(9):28-31. PubMed ID: 16438446
[TBL] [Abstract][Full Text] [Related]
10. European medical device regulation: a new era?
Donawa M
Med Device Technol; 2004 Dec; 15(10):30-1. PubMed ID: 16225282
[TBL] [Abstract][Full Text] [Related]
11. The Australian Medical Device Vigilance System.
Beech DR
Stud Health Technol Inform; 1996; 28():25-8. PubMed ID: 10172827
[TBL] [Abstract][Full Text] [Related]
12. Activities in other European countries.
Ecker W; De Roo R; Frellsen M; Gomes AF; Gutowski R
Stud Health Technol Inform; 1996; 28():119-23. PubMed ID: 10164088
[TBL] [Abstract][Full Text] [Related]
13. Ireland's competent authority initiatives.
Scully C
Stud Health Technol Inform; 1996; 28():101-11. PubMed ID: 10164084
[TBL] [Abstract][Full Text] [Related]
14. [The EU medical device market process and enlightenment for the review].
Luo Q
Zhongguo Yi Liao Qi Xie Za Zhi; 2014 May; 38(3):210-2. PubMed ID: 25241519
[TBL] [Abstract][Full Text] [Related]
15. [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]
16. [Discussion about the application of risk management to medical devices].
Xu FL
Zhongguo Yi Liao Qi Xie Za Zhi; 2006 Mar; 30(2):123-8. PubMed ID: 16830807
[TBL] [Abstract][Full Text] [Related]
17. Quality analysis of medical device vigilance reports.
Sievänen H; Pommelin P
Technol Health Care; 2003; 11(4):275-81. PubMed ID: 14600338
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Feds focus on medical devices.
Goldfarb B; Wolfberg D
JEMS; 1992 Jul; 17(7):35-8, 45-7. PubMed ID: 10120068
[No Abstract] [Full Text] [Related]
20. New medical devices reporting requirements.
Carley MM
Contemp Longterm Care; 1991 Dec; 14(12):66, 68. PubMed ID: 10117951
[No Abstract] [Full Text] [Related]
[Next] [New Search]
