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 *

389 related articles for article (PubMed ID: 16225272)

  • 21. Switzerland: one year's experience with new regulations and a new agency.
    Voelksen R
    Med Device Technol; 2003 Mar; 14(2):28-9. PubMed ID: 12698697
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Safety testing of medical devices: IEC 62353 explained.
    Backes J
    Med Device Technol; 2007; 18(7):46-7. PubMed ID: 18075136
    [TBL] [Abstract][Full Text] [Related]  

  • 23. How to kick-start your CAPA process.
    Peterson K
    Biomed Instrum Technol; 2005; 39(1):55-9. PubMed ID: 15742850
    [No Abstract]   [Full Text] [Related]  

  • 24. What is in the QSR/GMP?
    Bartoo G;
    IEEE Eng Med Biol Mag; 2004; 23(4):83-5. PubMed ID: 15508391
    [No Abstract]   [Full Text] [Related]  

  • 25. Beyond the US submisson process.
    Donawa M
    Med Device Technol; 2004 Apr; 15(3):30-2. PubMed ID: 15255536
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Validation.
    Isaacs A
    Med Device Technol; 2001 Dec; 12(10):38, 40. PubMed ID: 15966146
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The compatibility of standardisation and innovation.
    Moore R
    Med Device Technol; 2004 Nov; 15(9):28. PubMed ID: 16231785
    [No Abstract]   [Full Text] [Related]  

  • 28. How FDA-recognized standards impact users, manufacturers.
    Osborn D
    Biomed Instrum Technol; 2009; 43(2):156-7. PubMed ID: 19480488
    [No Abstract]   [Full Text] [Related]  

  • 29. 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]  

  • 30. [Importance of the Therapeutic Products Act for the ENT practitioner].
    Kaiser R; Ininger G; Stosslein E
    HNO; 2003 Jun; 51(6):513-24; quiz 525-6. PubMed ID: 12858855
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Managing changes during a clinical investigation, Part II.
    Donawa M
    Med Device Technol; 2003 Oct; 14(8):24-7. PubMed ID: 14603716
    [TBL] [Abstract][Full Text] [Related]  

  • 32. How are medical devices regulated in the European Union?
    French-Mowat E; Burnett J
    J R Soc Med; 2012 Apr; 105 Suppl 1(Suppl 1):S22-8. PubMed ID: 22508970
    [No Abstract]   [Full Text] [Related]  

  • 33. Effective risk management programmes.
    Donawa M
    Med Device Technol; 2004 May; 15(4):28-30. PubMed ID: 15303561
    [TBL] [Abstract][Full Text] [Related]  

  • 34. An important step forward in the global harmonisation of premarket review programmes.
    Donawa M
    Med Device Technol; 2001 Sep; 12(7):28-30. PubMed ID: 12938557
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. User reporting of medical device related incidents.
    Sievänen H
    Med Device Technol; 2003 May; 14(4):26-9. PubMed ID: 12774575
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A new guide to EMC.
    Harvey N
    Med Device Technol; 1997 Dec; 8(10):26-8. PubMed ID: 10176364
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Solving electromagnetic compatibility problems in medical equipment.
    Kirk S
    Med Device Technol; 1992; 3(1):27-30. PubMed ID: 10171584
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Combination products and the role of medical device firms.
    Etheredge R
    Biomed Instrum Technol; 2005; 39(2):143-6. PubMed ID: 15810788
    [No Abstract]   [Full Text] [Related]  

  • 40. Risk management.
    Bartoo G
    IEEE Eng Med Biol Mag; 2003; 22(4):166-70, 172. PubMed ID: 14515712
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 20.