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  1. IDRAS - Welcome to the i.DRAS GmbH website

    i.DRAS stands for international, intelligent, individual, innovative and independent solutions for your drug regulatory affairs projects
    human medicinal0
    veterinary medicinal products0

    www.i-dras.com - 2009-02-09
  2. PathSys

    pathsys
    lluorescence0
    oxicology0
    pathology working group0

    www.pathsys.com - 2009-02-03
  3. Horn Pharmaceutical Consulting - ASMF, Active Substance Master File, US-DMF, Drug Master File, Certificate of suitability, CEP, CTA ,Clinical Trial Applicat ...

    HORN Pharmaceutical Consulting provides regulatory and business advice to companies from the pharmaceutical, biotechnology and medical device industries.
    Biologic License Application0
    CMC-documents0
    European MAA0
    quality overall summaries0

    www.horn-pharma.de - 2009-02-13
  4. ERA Consulting Group - Regulatory Affairs Consulting for the Biopharmaceutical Industry

    Specialist regulatory affairs consulting services to pharmaceutical companies, including scientific and technical aspects, towards the development and ...
    biological medicinal products0
    clinical trial applications0

    www.eraconsulting.com - 2009-02-07
  5. Extedo GmbH: Home

    Extedo GmbH
    eCTD application0
    eCTD dossier0
    eCTD electronic0
    eCTD electronic Submissions0
    eCTD express0
    eCTD file0
    eCTD format0
    eCTD guidelines0
    eCTD lifecycle0
    eCTDmanager0

    iabg-lss.com - 2009-04-02
  6. Welcome to Design Space InPharmatics

    Design Space InPharmatics (DSI) is a CMC regulatory consultancy agency providing high-functionality user-configurable authoring tools and a range of development ...
    CMC Regulatory Strategy0
    CTD ProcessPro0
    Design Space InPharmatics0
    PharmWrite0
    Quality Modules0
    Zbyszewski0

    www.dsinpharmatics.com - 2009-02-11
  7. Robin Guy Consulting Toxicologist - DABT toxicology consultant, ICH, IND, GLP studies

    Robin Guy Consulting, preclinical toxicology safety assessment consultant for pharmaceuticals, biologics, food additives, ingredients, dietary supplements ...

    www.robinguy.com - 2009-02-04
  8. Medwise International - About Us

    Preparation of expert reviews of materials , chemical safety & toxicology
    Medwise consultancy0

    www.medwise-international.com - 2009-02-07
  9. CTD Quality Consulting - Common Technical Document Submissions Guidelines Courses

    CTD Quality Consulting provides expertise in preparing the Quality modules (CMC, Chemistry, Manufacturing, and Controls) for regulatory submissions of the ...
    CTD Module 20
    CTD Quality0
    MAA New Drug Applications0
    pre-meeting packages0

    www.ctdquality.com - 2009-02-05
  10. RegInfo

    RegInfo Törzskönyvezési és Informatikai Szolgáltató Kft. Tevékenységünk: Gyógyszeripari elektronikus dokumentációk előállítása Elektronikus dokumentumkezelés Törz ...

    www.reginfo.hu - 2009-04-08

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