BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

162 related articles for article (PubMed ID: 10155369)

  • 1. A new year's revelation: the boss needs training too.
    Donawa ME
    Med Device Technol; 1995; 6(1):11-3. PubMed ID: 10155369
    [TBL] [Abstract][Full Text] [Related]  

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

  • 3. Implementing a QA system in a small company.
    Carentz JY
    Med Device Technol; 1995 Apr; 6(3):30-4. PubMed ID: 10155380
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Validation and Six Sigma.
    Barry E
    Med Device Technol; 2008; 19(7):36, 38-40. PubMed ID: 19133627
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Controlling the quality of raw materials.
    Donawa ME
    Med Device Technol; 1998; 9(1):12-5. PubMed ID: 10176139
    [TBL] [Abstract][Full Text] [Related]  

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

  • 7. 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]  

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

  • 9. Total quality in health care.
    Brannan KM
    Hosp Mater Manage Q; 1998 May; 19(4):1-8. PubMed ID: 10178544
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The quality planning conundrum.
    Donawa ME
    Med Device Technol; 1999; 10(6):14-6. PubMed ID: 10623345
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. ISO 9000:2000 revisions and their implications.
    Sim P
    Med Device Technol; 2000 May; 11(4):45-7. PubMed ID: 11010320
    [TBL] [Abstract][Full Text] [Related]  

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

  • 14. 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]  

  • 15. Complying with US and European change control requirements, Part I.
    Donawa ME
    Med Device Technol; 1997 Oct; 8(8):10-3. PubMed ID: 10174270
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Creating win-win customer-supplier partnerships.
    Willis AK
    Hosp Mater Manage Q; 1998 Feb; 19(3):15-22. PubMed ID: 10176282
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Avoiding unreasonable reliance on subcontractor certification.
    Donawa ME
    Med Device Technol; 1998 Dec; 9(10):9-12. PubMed ID: 10344878
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Learning to lead at Toyota.
    Spear SJ
    Harv Bus Rev; 2004 May; 82(5):78-86, 151. PubMed ID: 15146738
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Meeting European and US requirements for design and development documentation, Part I.
    Donawa ME
    Med Device Technol; 1996 Nov; 7(9):12-5. PubMed ID: 10163673
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.