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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

392 related articles for article (PubMed ID: 16282661)

  • 1. Software process improvement for the medical industry.
    McCaffery F; Donnelly P; McFall D; Wilkie FG
    Stud Health Technol Inform; 2005; 117():117-24. PubMed ID: 16282661
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The role of the notified body in the CE marking of medical devices.
    Rader J; Schaff P; Kreinberg W
    Health Estate; 1999 Apr; 53(3):14-6. PubMed ID: 10387568
    [No Abstract]   [Full Text] [Related]  

  • 3. 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]  

  • 4. Technology assessment of medical devices at the Center for Devices and Radiological Health.
    Kessler L; Richter K
    Am J Manag Care; 1998 Sep; 4 Spec No():SP129-35. PubMed ID: 10185989
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Medical device regulation for manufacturers.
    McAllister P; Jeswiet J
    Proc Inst Mech Eng H; 2003; 217(6):459-67. PubMed ID: 14702983
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 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. [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]  

  • 10. Mutual recognition of pharmaceutical good manufacturing practice inspection reports, medical device quality system audit reports, and certain medical device product evaluation reports between the United States and the European Community--FDA. Final rule.
    Fed Regist; 1998 Nov; 63(215):60122-64. PubMed ID: 10187390
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Achieving systematic compliance with the Medical Device Directive.
    Lally R
    Med Device Technol; 1996 Sep; 7(7):28-33. PubMed ID: 10172791
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Strategic planning for U.S. premarket approval submissions.
    Donawa M
    Med Device Technol; 2006 Sep; 17(7):21-3. PubMed ID: 17039953
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Quality assurance for antimicrobial devices.
    Bruenke J; Aldinger U; Bechert T; Steinruecke P
    Med Device Technol; 2006; 17(9):16-8. PubMed ID: 17240681
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Software as a medical device: regulatory critical issues.
    Pelayo S; Bras Da Costa S; Leroy N; Loiseau S; Beuscart-Zephir MC
    Stud Health Technol Inform; 2013; 183():337-42. PubMed ID: 23388310
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Product-based Safety Certification for Medical Devices Embedded Software.
    Neto JA; Figueiredo Damásio J; Monthaler P; Morais M
    Stud Health Technol Inform; 2015; 216():227-31. PubMed ID: 26262044
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The Center for Devices and Radiological health: an update.
    Donawa M
    Med Device Technol; 2001 Dec; 12(10):24, 26-7. PubMed ID: 15966141
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Utility of medical devices: approaches to planning and conducting clinical trials].
    Ziegler A; Heimerl A; Krockenberger K; Hemmelmann C
    Z Evid Fortbild Qual Gesundhwes; 2012; 106(5):322-31; discussion 332. PubMed ID: 22818149
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Guidance on submitting quality system information.
    Donawa ME
    Med Device Technol; 2004 Mar; 15(2):24-7. PubMed ID: 15154336
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Standards used in the regulation of medical device in USA].
    Hu W; Gu H
    Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi; 2007 Nov; 21(11):1263-7. PubMed ID: 18069490
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 20.