Showing 1 - 9 results of 9 for search '"Medical instruments and apparatus industry Law and legislation United States"', query time: 0.06s Refine Results
  1. 1
    Reauthorization of the Medical Device User Fee and Modernization Act hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Tenth Congress, first session, May 16, 2007.

    Reauthorization of the Medical Device User Fee and Modernization Act hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, On... by United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health

    Published: U.S. G.P.O., 2008
    Subjects: “…Medical instruments and apparatus industry Law and legislation United States.…”
    Get full text
    Government Document Online Book
    Save to List
    Saved in:
  2. 2
    An Act to Amend the Federal Food, Drug, and Cosmetic Act with Respect to Medical Device User Fees.

    An Act to Amend the Federal Food, Drug, and Cosmetic Act with Respect to Medical Device User Fees. by United States

    Subjects: “…Medical instruments and apparatus industry Law and legislation United States.…”
    Get full text
    Get full text
    Government Document Online Book
    Save to List
    Saved in:
  3. 3
    An Act to Repeal an Unnecessary Medical Device Reporting Requirement.

    An Act to Repeal an Unnecessary Medical Device Reporting Requirement.

    Subjects: “…Medical instruments and apparatus industry Law and legislation United States.…”
    Get full text
    Get full text
    Government Document Online Book
    Save to List
    Saved in:
  4. 4
    Examining FDA's Medical Device User Fee Program : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Fifteenth Congress, first session, March 28, 2017.

    Examining FDA's Medical Device User Fee Program : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Fifteenth... by United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health

    Subjects: “…Medical instruments and apparatus industry Law and legislation United States.…”
    Get full text
    Government Document Online Book
    Save to List
    Saved in:
  5. 5
    FDA regulation of medical devices /

    FDA regulation of medical devices / by Thompson, Bradley Merrill

    Published: Interpharm Press, 1995
    Subjects: “…Medical instruments and apparatus industry Law and legislation United States.…”
    Book
    Save to List
    Saved in:
  6. 6
    Reauthorization of MDUFA : what it means for jobs, innovation, and patients : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Twelfth Congress, second session, February 15, 2012.

    Reauthorization of MDUFA : what it means for jobs, innovation, and patients : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representa... by United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health

    Subjects: “…Medical instruments and apparatus industry Law and legislation United States.…”
    Get full text
    Government Document Online Book
    Save to List
    Saved in:
  7. 7
    Discussion drafts concerning Prescription Drug User Fee Act reauthorization, Medical Device User Fee and Modernization Act reauthorization, drug safety, and certain pediatric pharmaceutical and device legislation hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Tenth Congress, first session, June 12, 2007.

    Discussion drafts concerning Prescription Drug User Fee Act reauthorization, Medical Device User Fee and Modernization Act reauthorization, drug safety, and certain pediatric pharm... by United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health

    Published: U.S. G.P.O., 2008
    Subjects: “…Medical instruments and apparatus industry Law and legislation United States.…”
    Get full text
    Government Document Online Book
    Save to List
    Saved in:
  8. 8
    The FDA and worldwide quality system requirements guidebook for medical devices /

    The FDA and worldwide quality system requirements guidebook for medical devices / by Daniel, Amiram, Kimmelman, Ed, ProQuest Ebook Subscriptions

    Published: ASQ Quality Press, 2008
    Subjects: “…Medical instruments and apparatus industry Law and legislation United States.…”
    Get full text
    Online Book
    Save to List
    Saved in:
  9. 9
    FDA user fees and the regulation of drugs, biologics, and devices : comparative analysis of S. 3187 and H.R. 5651 /

    FDA user fees and the regulation of drugs, biologics, and devices : comparative analysis of S. 3187 and H.R. 5651 / by Thaul, Susan

    Subjects: “…Medical instruments and apparatus industry Law and legislation United States.…”
    Get full text
    Government Document Online
    Save to List
    Saved in:

Search Tools: