BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

234 related articles for article (PubMed ID: 3781809)

  • 1. Marketing approval for the lithotripter.
    Nightingale SL; Young FE
    Isr J Med Sci; 1986; 22(7-8):519-23. PubMed ID: 3781809
    [TBL] [Abstract][Full Text] [Related]  

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

  • 3. FDA marketing claims, and the practitioner.
    Runner S
    J Evid Based Dent Pract; 2006 Mar; 6(1):19-23. PubMed ID: 17138391
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Lessons learned from independent central review.
    Ford R; Schwartz L; Dancey J; Dodd LE; Eisenhauer EA; Gwyther S; Rubinstein L; Sargent D; Shankar L; Therasse P; Verweij J
    Eur J Cancer; 2009 Jan; 45(2):268-74. PubMed ID: 19101138
    [TBL] [Abstract][Full Text] [Related]  

  • 5. What physicians should know about the regulation of Obstetric and Gynecologic Medical Devices.
    Yin L
    J Reprod Med; 1983 Jan; 28(1):3-11. PubMed ID: 6834344
    [TBL] [Abstract][Full Text] [Related]  

  • 6. New drug, antibiotic, and biological drug product regulations; accelerated approval--FDA. Final rule.
    Fed Regist; 1992 Dec; 57(239):58942-60. PubMed ID: 10123232
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cochlear implants: overview of safety and effectiveness. The FDA evaluation.
    Yin L; Segerson DA
    Otolaryngol Clin North Am; 1986 May; 19(2):423-33. PubMed ID: 3520445
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Gastroenterology and urology devices; reclassification of the extracorporeal shock wave lithotripter. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 2000 Aug; 65(154):48609-12. PubMed ID: 11067714
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Medical devices; investigational device exemptions--FDA. Final rule.
    Fed Regist; 1998 Nov; 63(225):64617-26. PubMed ID: 10338870
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Safe Medical Devices Act: management guidance for hospital compliance with the new FDA requirements.
    Alder HC
    Hosp Technol Ser; 1993 Oct; 12(11):1-27. PubMed ID: 10129209
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Medical devices; investigational device exemptions--FDA. Proposed rule.
    Fed Regist; 1998 Jul; 63(135):38131-8. PubMed ID: 10181246
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Medical device reporting: manufacturer reporting, importer reporting, user facility reporting, and distributor reporting--FDA. Direct final rule.
    Fed Regist; 1998 May; 63(91):26069-77. PubMed ID: 10179334
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The role of the FDA in the effort against AIDS.
    Young FE
    Public Health Rep; 1988; 103(3):242-5. PubMed ID: 3131814
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The role of the U.S. Food and Drug Administration in device evaluation and monitoring.
    ; Diehl DL; Tierney WM; Adler DG; Conway JD; Farraye FA; Kantsevoy SV; Kaul V; Kethu SR; Kwon RS; Mamula P; Pedrosa MC; Rodriguez SA
    Gastrointest Endosc; 2010 Jul; 72(1):5-10. PubMed ID: 20421100
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Making sense of the food and drug administration.
    Connor JA
    Semin Pediatr Surg; 2006 Nov; 15(4):293-301. PubMed ID: 17055960
    [TBL] [Abstract][Full Text] [Related]  

  • 16. US FDA perspective on the regulations of medical-grade polymers: cyanoacrylate polymer medical device tissue adhesives.
    Mattamal GJ
    Expert Rev Med Devices; 2008 Jan; 5(1):41-9. PubMed ID: 18095895
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Medical devices; device tracking; new orders to manufacturers--FDA. Notice.
    Fed Regist; 1998 Mar; 63(42):10638-40. PubMed ID: 10177504
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The issue of a U.S. Food and Drug Administration moratorium on the use of the pulmonary artery catheter.
    Sprung CL; Eidelman LA
    New Horiz; 1997 Aug; 5(3):277-80. PubMed ID: 9259343
    [TBL] [Abstract][Full Text] [Related]  

  • 19. New obstacles in the path of marketing new medical devices.
    Bucci VA; Reiss JB; Hall NC
    J Health Care Technol; 1985; 2(2):81-96. PubMed ID: 10300491
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Administrative practices and procedures; internal review of decisions--FDA. Final rule.
    Fed Regist; 1998 Nov; 63(222):63978-82. PubMed ID: 10339046
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.