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 *

129 related articles for article (PubMed ID: 10155394)

  • 21. Not long to go: the end of the transition period approaches.
    Cutler IR
    Med Device Technol; 1997 Nov; 8(9):28-30. PubMed ID: 10174627
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Notifying the competent authorities.
    Donawa ME
    Med Device Technol; 1998 Nov; 9(9):12-6. PubMed ID: 10344879
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Meeting European and US requirements for design and development documentation, Part II.
    Donawa ME
    Med Device Technol; 1996 Dec; 7(10):10-5. PubMed ID: 10164052
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Implementing new European vigilance procedures.
    Donawa M
    Med Device Technol; 2007; 18(7):34, 36-7. PubMed ID: 18075133
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A logical approach to process validation.
    Donawa ME
    Med Device Technol; 1995 Mar; 6(2):13-8. PubMed ID: 10155374
    [TBL] [Abstract][Full Text] [Related]  

  • 26. European standards and the In Vitro Diagnostic Directive: current status.
    Suppo M
    Med Device Technol; 1996; 7(6):26-9. PubMed ID: 10172759
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Management responsibility.
    Donawa ME
    Med Device Technol; 1995 Jun; 6(5):11-3. PubMed ID: 10155388
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Final FDA inspection manual.
    Donawa M
    Med Device Technol; 2001 Apr; 12(3):29-32. PubMed ID: 11547684
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Review of the Medical Device Directive.
    Donawa M
    Med Device Technol; 2003 Mar; 14(2):20-3. PubMed ID: 12698694
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Notified bodies. Questions and answers.
    Lindley E
    Med Device Technol; 1995 Mar; 6(2):38-43. PubMed ID: 10155376
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Diagnostic kits in parasitology: which controls?].
    Rossi P
    Parassitologia; 2004 Jun; 46(1-2):145-9. PubMed ID: 15305705
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. 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]  

  • 35. A packaging update. Recycling, testing, and pricing.
    Baker MC
    Med Device Technol; 1995 May; 6(4):31-3. PubMed ID: 10155385
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Update on the forthcoming European Clinical Investigation Standards.
    Donawa M
    Med Device Technol; 2002 Sep; 13(7):24-5. PubMed ID: 12397830
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Clinical evaluation or investigation?
    O'Connor N
    Med Device Technol; 1998 Oct; 9(8):30-3. PubMed ID: 10186989
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. 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]  

  • 40. The review of the RoHS Directive.
    Howes K
    Med Device Technol; 2006; 17(9):24, 26. PubMed ID: 17240683
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.