318 related articles for article (PubMed ID: 10176143)
1. Marketing medical devices in Japan.
Ohashi J
Med Device Technol; 1998; 9(1):32-3, 36-7. PubMed ID: 10176143
[TBL] [Abstract][Full Text] [Related]
2. Design and implementation of a portal for the medical equipment market: MEDICOM.
Palamas S; Kalivas D; Panou-Diamandi O; Zeelenberg C; van Nimwegen C
J Med Internet Res; 2001; 3(4):E32. PubMed ID: 11772547
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. The responsibilities of importers and distributors.
Donawa ME
Med Device Technol; 1998 Sep; 9(7):12-4, 16-8. PubMed ID: 10186979
[TBL] [Abstract][Full Text] [Related]
5. Meeting US and European supplier control requirements.
Donawa M
Med Device Technol; 2009; 20(3):24-7. PubMed ID: 19626952
[TBL] [Abstract][Full Text] [Related]
6. Process validation: harmonizing the requirements.
Donawa ME
Med Device Technol; 1998 Oct; 9(8):13-6. PubMed ID: 10186986
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. Tracking and surveillance of patients with medical devices and implants.
Morgan RW
Med Device Technol; 1993; 4(1):38-43. PubMed ID: 10171686
[TBL] [Abstract][Full Text] [Related]
10. European requirements for product returns.
Donawa M
Med Device Technol; 2005 Nov; 16(9):28-31. PubMed ID: 16438446
[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. Organising European technical documentation to avoid duplication.
Donawa M
Med Device Technol; 2006 Apr; 17(3):29-31. PubMed ID: 16736662
[TBL] [Abstract][Full Text] [Related]
13. Use and recognition of consensus standards in US premarket submissions.
Donawa ME
Med Device Technol; 1999 Mar; 10(2):13-7. PubMed ID: 10387610
[TBL] [Abstract][Full Text] [Related]
14. The impact of the new quality management system standards on the CE-marking process.
Donawa M
Med Device Technol; 2001; 12(1):34-9. PubMed ID: 11317864
[TBL] [Abstract][Full Text] [Related]
15. Notifying the competent authorities.
Donawa ME
Med Device Technol; 1998 Nov; 9(9):12-6. PubMed ID: 10344879
[TBL] [Abstract][Full Text] [Related]
16. [Introduction of innovative high-risk medical devices in Europe: are clinical efficacy and safety guaranteed?].
Stordeur S; Vinck I; Neyt M; Van Brabandt H; Hulstaert F
Rev Epidemiol Sante Publique; 2013 Apr; 61(2):105-10. PubMed ID: 23477881
[TBL] [Abstract][Full Text] [Related]
17. [The dependability and safety of biomaterials and medical devices].
Li Q
Zhongguo Yi Liao Qi Xie Za Zhi; 2005 Jan; 29(1):46-9. PubMed ID: 15875695
[TBL] [Abstract][Full Text] [Related]
18. Medical device problem reporting for the betterment of healthcare.
Health Devices; 1998 Aug; 27(8):277-92. PubMed ID: 9743900
[TBL] [Abstract][Full Text] [Related]
19. Selecting a sterilisation subcontractor.
Donawa M
Med Device Technol; 2001 Mar; 12(2):26-9. PubMed ID: 11317837
[TBL] [Abstract][Full Text] [Related]
20. Europe plans to strengthen surveillance system for medical devices, MPs are told.
O'Dowd A
BMJ; 2012 Jun; 344():e4179. PubMed ID: 22705817
[No Abstract] [Full Text] [Related]
[Next] [New Search]
