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 *

124 related articles for article (PubMed ID: 10163367)

  • 1. The importance of being authorized.
    Donawa ME
    Med Device Technol; 1996 Apr; 7(3):11-3. PubMed ID: 10163367
    [TBL] [Abstract][Full Text] [Related]  

  • 2. IVD authorized representatives.
    Donawa ME
    Med Device Technol; 2003 May; 14(4):19-21. PubMed ID: 12774572
    [TBL] [Abstract][Full Text] [Related]  

  • 3. EC declaration of conformity.
    Donawa ME
    Med Device Technol; 1996 May; 7(4):10-2. PubMed ID: 10163370
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Implementation of the medical device directives in Italy.
    Donawa ME
    Med Device Technol; 2002 Jun; 13(5):26-8. PubMed ID: 12116733
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Risk analysis: a standard approach? (Part II).
    Donawa ME
    Med Device Technol; 1995 May; 6(4):10-2. PubMed ID: 10155382
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Risk analysis: a standard approach? (Part I).
    Donawa ME
    Med Device Technol; 1995 Apr; 6(3):11-4. PubMed ID: 10172443
    [TBL] [Abstract][Full Text] [Related]  

  • 8. New Italian device registration requirements.
    Donawa M
    Med Device Technol; 2008; 19(3):26, 28-9, 31. PubMed ID: 18557406
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Legal aspects of E-HEALTH.
    Callens S; Cierkens K
    Stud Health Technol Inform; 2008; 141():47-56. PubMed ID: 18953124
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Notified body consensus statements.
    Donawa M
    Med Device Technol; 1999 Nov; 10(9):46-9, 51. PubMed ID: 10724656
    [TBL] [Abstract][Full Text] [Related]  

  • 12. European Animal Tissue Directive.
    Donawa M
    Med Device Technol; 2004; 15(1):28-31. PubMed ID: 14994636
    [TBL] [Abstract][Full Text] [Related]  

  • 13. European and US quality system requirements for packaging.
    Donawa ME
    Med Device Technol; 1997 May; 8(4):12-4, 16-7. PubMed ID: 10167684
    [TBL] [Abstract][Full Text] [Related]  

  • 14. European requirements for product returns.
    Donawa M
    Med Device Technol; 2005 Nov; 16(9):28-31. PubMed ID: 16438446
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. The proposed in vitro diagnostic directive.
    Donawa ME
    Med Device Technol; 1995 Sep; 6(7):12-6. PubMed ID: 10155394
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Using and controlling subcontractors.
    Burton W
    Med Device Technol; 1997 Dec; 8(10):14-6. PubMed ID: 10176362
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 7.