BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

210 related articles for article (PubMed ID: 10186979)

  • 1. 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]  

  • 2. Marketing medical devices in Japan.
    Ohashi J
    Med Device Technol; 1998; 9(1):32-3, 36-7. PubMed ID: 10176143
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Differing definitions of manufacturer.
    Donawa ME
    Med Device Technol; 1998; 9(6):14-7. PubMed ID: 10182120
    [TBL] [Abstract][Full Text] [Related]  

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

  • 6. Process validation: harmonizing the requirements.
    Donawa ME
    Med Device Technol; 1998 Oct; 9(8):13-6. PubMed ID: 10186986
    [TBL] [Abstract][Full Text] [Related]  

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

  • 8. User reporting systems.
    Donawa ME
    Med Device Technol; 1997 Dec; 8(10):10-2. PubMed ID: 10176361
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Understanding US labelling requirements.
    Donawa M
    Med Device Technol; 2005 Sep; 16(7):21-3. PubMed ID: 16259155
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Implementation of the Medical Device Directive in Italy.
    Donawa ME
    Med Device Technol; 1998 May; 9(4):33-5. PubMed ID: 10180744
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Organising European technical documentation to avoid duplication.
    Donawa M
    Med Device Technol; 2006 Apr; 17(3):29-31. PubMed ID: 16736662
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Tracking and surveillance of patients with medical devices and implants.
    Morgan RW
    Med Device Technol; 1993; 4(1):38-43. PubMed ID: 10171686
    [TBL] [Abstract][Full Text] [Related]  

  • 14. German law: the differences.
    Müller-Lierheim WG
    Med Device Technol; 1997 Nov; 8(9):38-40. PubMed ID: 10174630
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Sterile by any other name.
    Donawa ME
    Med Device Technol; 1996; 7(1):12-5. PubMed ID: 10172722
    [TBL] [Abstract][Full Text] [Related]  

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

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

  • 18. Design and implementation of a portal for the medical equipment market: MEDICOM.
    Palamas S; Kalivas D; Panou-Diamandi O; Zeelenberg C; van Nimwegen C
    J Med Internet Res; 2001; 3(4):E32. PubMed ID: 11772547
    [TBL] [Abstract][Full Text] [Related]  

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

  • 20. Testing for technical files: avoiding too little and too much.
    Clifford A
    Med Device Technol; 1998 Sep; 9(7):30-1. PubMed ID: 10186981
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.