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  1. Capamed Inc

    You are a provider of medical devices, in-vitro-diagnostics, active pharmaceutical ingredients, or a supplier to the pharmaceutical industry, or active in the ...
    pharma2
    biotech2
    API2
    FDA2
    Validation2
    GMP2
    IDE2
    medical device2
    qualification2
    quality management2
    PMA1
    cGMP1
    GCP1
    CAPA1
    QSR1
    ISO 134851
    BPC1
    510k1
    FDA approval1
    software validation1
    21 CFR 111
    warning letter1
    FDA inspection1
    FDA audit1
    21 CFR 8201

    www.capamed.com - 2009-02-10

  2. Noblitt & Rueland Home Page, FDA & International Consulting & Training Services

    FDA GMP, QSR, Design Control, software development, software validation, V&V, risk, hazard, submissions, 510(k), IDE, PMA, consulting and training.
    software development3
    pharmaceutical3
    submission2
    risk assessment2
    medical devices2
    IDE2
    medical device2
    submissions2
    FTA1
    risk analysis1
    PMA1
    FMEA1
    QSR1
    CE Mark1
    hazard analysis1
    510 k1
    510k1
    software validation1
    V&V1
    warning letter1
    software verification1
    Design Control1
    GMP audits1
    FDA inspection1
    design controls1
    EN 460011
    GMP audit1
    FDA 4831
    QSIT1
    FDA GMP1
    verification & validation1

    www.cemark.net - 2009-02-14

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