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 *

150 related articles for article (PubMed ID: 23804688)

  • 1. Design control requirements for medical device development.
    Kinsel D
    World J Pediatr Congenit Heart Surg; 2012 Jan; 3(1):77-81. PubMed ID: 23804688
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. Implementing the new quality system requirements: design controls.
    Stoeger KJ
    Biomed Instrum Technol; 1997; 31(2):119-27. PubMed ID: 9099433
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Standards for humidification and filtration devices.
    Stevens J
    Respir Care Clin N Am; 2006 Jun; 12(2):203-32. PubMed ID: 16828691
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Understanding the regulatory requirements for dialysate.
    Ward RA
    Nephrol News Issues; 1991 Jan; 5(1):13, 15. PubMed ID: 1961262
    [TBL] [Abstract][Full Text] [Related]  

  • 7. An overview of FDA regulatory requirements for new medical devices.
    Sucher JF; Jones SL; Montoya ID
    Expert Opin Med Diagn; 2009 Jan; 3(1):5-11. PubMed ID: 23495960
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Design control considerations for biologic-device combination products.
    Anderson D; Liu R; Anand Subramony J; Cammack J
    Adv Drug Deliv Rev; 2017 Mar; 112():101-105. PubMed ID: 28088344
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Medical devices; current good manufacturing practice (CGMP) final fule; quality system regulation--FDA. Final rule.
    Fed Regist; 1996 Oct; 61(195):52602-62. PubMed ID: 10168287
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The use of total quality principles to achieve regulatory compliance in research laboratories.
    Hynes MD
    Qual Assur; 1995 Mar; 4(1):34-40. PubMed ID: 8520863
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Mutual recognition of pharmaceutical good manufacturing practice inspection reports, medical device quality system audit reports, and certain medical device product evaluation reports between the United States and the European Community--FDA. Final rule.
    Fed Regist; 1998 Nov; 63(215):60122-64. PubMed ID: 10187390
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Risk management frameworks for human health and environmental risks.
    Jardine C; Hrudey S; Shortreed J; Craig L; Krewski D; Furgal C; McColl S
    J Toxicol Environ Health B Crit Rev; 2003; 6(6):569-720. PubMed ID: 14698953
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Regulation of medical devices in radiology: current standards and future opportunities.
    Smith JJ
    Radiology; 2001 Feb; 218(2):329-35. PubMed ID: 11161144
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Facilities strive to comply with new Act. The long-term effects of the Safe Medical Devices Act are still unknown.
    Schuster DK; Butler KH
    Health Prog; 1993 May; 74(4):53-7. PubMed ID: 10125364
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Medical device reporting: the US final rule.
    Donawa ME
    Med Device Technol; 1996 Mar; 7(2):14-6, 18, 20-1. PubMed ID: 10159867
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Design and implementation of an audit trail in compliance with US regulations.
    Jiang K; Cao X
    Clin Trials; 2011 Oct; 8(5):624-33. PubMed ID: 21900341
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.