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.
820 related articles for article (PubMed ID: 19708431)
1. Medical Device Manufacturing and Medical Device Reports (MDR). Arellano V Insight; 2009; 34(3):24-5. PubMed ID: 19708431 [No Abstract] [Full Text] [Related]
2. Medical device reporting: the US final rule. Donawa ME Med Device Technol; 1996 Mar; 7(2):14-6, 18, 20-1. PubMed ID: 10159867 [TBL] [Abstract][Full Text] [Related]
3. How do regulatory agencies ensure the release of a safe medical device? Haggar B Clin Perform Qual Health Care; 1999; 7(2):100-3. PubMed ID: 10747561 [TBL] [Abstract][Full Text] [Related]
4. Ensuring safe and effective medical devices. Feigal DW; Gardner SN; McClellan M N Engl J Med; 2003 Jan; 348(3):191-2. PubMed ID: 12529457 [No Abstract] [Full Text] [Related]
5. Myths and realities in medical packaging. Pilchik R Med Device Technol; 2003 Mar; 14(2):16-7. PubMed ID: 12698692 [TBL] [Abstract][Full Text] [Related]
6. Computerized medical device tracking--ways to comply with SMDA (Safe Medical Devices Act of 1990). Landis D Healthc Inform; 1992 Jul; 9(7):36, 38, 40-2. PubMed ID: 10119858 [No Abstract] [Full Text] [Related]
7. Devices and the food and drug administration. Phillips SJ; Phillips RS Artif Organs; 2005 May; 29(5):363-5. PubMed ID: 15854210 [No Abstract] [Full Text] [Related]
8. 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]
9. 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]
10. 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]
11. Pharmaceuticals and medical devices: medical devices. Berry MD Issue Brief Health Policy Track Serv; 2013 Dec; ():1-49. PubMed ID: 24482892 [No Abstract] [Full Text] [Related]
12. Postmarketing surveillance of medical devices--filling in the gaps. Resnic FS; Normand SL N Engl J Med; 2012 Mar; 366(10):875-7. PubMed ID: 22332950 [No Abstract] [Full Text] [Related]
13. The impact of FDA reform. Trunzo J Med Device Technol; 2003 Apr; 14(3):36-7. PubMed ID: 12789699 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. Medical device vigilance at FDA. Gross TP; Kessler LG Stud Health Technol Inform; 1996; 28():17-24. PubMed ID: 10164091 [TBL] [Abstract][Full Text] [Related]
16. FDA is gold standard of review. Leahey MB BMJ; 2010 Dec; 341():c7004. PubMed ID: 21139000 [No Abstract] [Full Text] [Related]
17. Medical device regulatory landscape: the imperative of finding balance. Kaplan AV; Williams DO Circ Cardiovasc Interv; 2012 Feb; 5(1):2-5. PubMed ID: 22337999 [No Abstract] [Full Text] [Related]
18. MEDWATCH: the new FDA medical products reporting program. Kennedy DL Respir Care; 1993 Oct; 38(10):1077-80. PubMed ID: 10145891 [No Abstract] [Full Text] [Related]
19. Medical devices; medical device user facility and manufacturer reporting, certification and registration; Office of Management and Budget approval; extension of effective date--FDA. Final rule; notification of approval of information collection requirements. Fed Regist; 1996 Apr; 61(71):16043-5. PubMed ID: 10157704 [No Abstract] [Full Text] [Related]
20. FDA pilot programme in support of global harmonisation. Donawa ME Med Device Technol; 2003 Nov; 14(9):32-4. PubMed ID: 14682021 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]