BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

221 related articles for article (PubMed ID: 10173028)

  • 1. Controls on clinical investigations in Europe: national differences.
    Sorrel S
    Med Device Technol; 1997 May; 8(4):22-6. PubMed ID: 10173028
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Conducting clinical studies in Italy.
    Donawa M
    Med Device Technol; 2005 Oct; 16(8):21-4. PubMed ID: 16355966
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. The regulatory situation in central and eastern Europe.
    Clarke JA
    Med Device Technol; 1997 Apr; 8(3):26-9. PubMed ID: 10173027
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Risk management of European device clinical studies.
    Donawa M
    Med Device Technol; 2007; 18(2):39-42. PubMed ID: 17494500
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Notified Body guidance on clinical evaluation.
    Donawa M
    Med Device Technol; 2000 Sep; 11(7):26-8. PubMed ID: 15326742
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical investigation of medical devices.
    Stewart RR
    Med Device Technol; 1995 Jun; 6(5):36-40. PubMed ID: 10155392
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. European Community Medical Device Directives.
    Health Trends; 1992; 24(1):6-7. PubMed ID: 10171283
    [No Abstract]   [Full Text] [Related]  

  • 12. French homologation for medical devices: past and future.
    Rader J
    Med Device Technol; 1993 Apr; 4(3):26-30. PubMed ID: 10171652
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Clinical trials of medical devices].
    Villars F; Pariente JL; Conort P
    Prog Urol; 2005 Nov; 15(5):996-9. PubMed ID: 16475664
    [No Abstract]   [Full Text] [Related]  

  • 14. When to conduct a clinical trial.
    Boutrand JP
    Med Device Technol; 2004 Oct; 15(8):28-31. PubMed ID: 16225271
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. CE marking & the MDD: what difference will the new regulations make?
    Lindley E
    EDTNA ERCA J; 1996; 22(1):29-30. PubMed ID: 10723308
    [TBL] [Abstract][Full Text] [Related]  

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

  • 18. Successful recruitment for medical device clinical studies.
    Donawa M
    Med Device Technol; 2004 Oct; 15(8):25-7. PubMed ID: 16225270
    [TBL] [Abstract][Full Text] [Related]  

  • 19. ["Medical devices and European regulations"].
    Fleur F
    Ann Pharm Fr; 1997; 55(2):73-6. PubMed ID: 9181704
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The biological evaluation of medical devices used in dentistry. The influence of the European Union on the preclinical screening of dental materials.
    Schmalz G; Browne RM
    Int Dent J; 1995 Aug; 45(4):275-8. PubMed ID: 7558367
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.