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.
389 related articles for article (PubMed ID: 16225272)
41. Testing for technical files: avoiding too little and too much. Clifford A Med Device Technol; 1998 Sep; 9(7):30-1. PubMed ID: 10186981 [TBL] [Abstract][Full Text] [Related]
42. Regulation of medical devices outside the European Union. Lamph S J R Soc Med; 2012 Apr; 105 Suppl 1(Suppl 1):S12-21. PubMed ID: 22508968 [No Abstract] [Full Text] [Related]
43. [How to apply for european CE certification for Chinese medical device manufacturers]. Xu XG Zhongguo Yi Liao Qi Xie Za Zhi; 2006 Nov; 30(6):453-6. PubMed ID: 17300018 [TBL] [Abstract][Full Text] [Related]
44. Regulation of medical devices in the European Union. Chai J J Leg Med; 2000 Dec; 21(4):537-56. PubMed ID: 11194571 [No Abstract] [Full Text] [Related]
45. 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]
46. Evidence-based medicine and drug-eluting stents. O'Dwyer J Med Device Technol; 2004 May; 15(4):34-7. PubMed ID: 15303564 [TBL] [Abstract][Full Text] [Related]
47. Successful recruitment for medical device clinical studies. Donawa M Med Device Technol; 2004 Oct; 15(8):25-7. PubMed ID: 16225270 [TBL] [Abstract][Full Text] [Related]
48. The US medical device bundling policy. Donawa M Med Device Technol; 2004 Nov; 15(9):25-7. PubMed ID: 16231784 [TBL] [Abstract][Full Text] [Related]
50. Medical device directive: preparing for the amendments. Donawa M Med Device Technol; 2000; 11(1):40-5. PubMed ID: 10915484 [TBL] [Abstract][Full Text] [Related]
51. US regulation of combination products. Donawa M Med Device Technol; 2009 Oct; 20(6):22, 24-5. PubMed ID: 20302139 [TBL] [Abstract][Full Text] [Related]
52. When to conduct a clinical trial. Boutrand JP Med Device Technol; 2004 Oct; 15(8):28-31. PubMed ID: 16225271 [TBL] [Abstract][Full Text] [Related]
53. US importer and distributor requirements. Donawa M Med Device Technol; 2005 Jun; 16(5):25-7. PubMed ID: 15984543 [TBL] [Abstract][Full Text] [Related]
54. User reporting systems. Donawa ME Med Device Technol; 1997 Dec; 8(10):10-2. PubMed ID: 10176361 [TBL] [Abstract][Full Text] [Related]
55. 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]
56. New trends in biological evaluation of medical devices. Bollen LS Med Device Technol; 2005 Jun; 16(5):10-5. PubMed ID: 15984539 [TBL] [Abstract][Full Text] [Related]
57. The evolving process of European combination product review, Part II. Donawa ME Med Device Technol; 2008; 19(7):26, 28-31. PubMed ID: 19133625 [TBL] [Abstract][Full Text] [Related]
58. Current and future issues in sensitisation testing. Eloy R; Charton-Picard F; Delubac C; Kergozien S Med Device Technol; 2001 Sep; 12(7):12-5. PubMed ID: 12938553 [TBL] [Abstract][Full Text] [Related]
59. New guidance on the European declaration of conformity. Donawa M Med Device Technol; 2001 May; 12(4):21-4. PubMed ID: 11521650 [No Abstract] [Full Text] [Related]
60. FDA is gold standard of review. Leahey MB BMJ; 2010 Dec; 341():c7004. PubMed ID: 21139000 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]