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  1. Pharmanalytical Consulting Services

    Pharmanalytical Consulting, Inc. is committed to the success of our customers in emerging, start-up and resource-limited pharmaceutical companies. Our ...
    chemical manufacturing control0
    contract resource organization0

    www.pharmanalytical.com - 2009-02-09
  2. B&H Consulting Services, Inc.

    B&H Consulting Services, Inc. is committed to assisting health sciences companies effectively meet their global Regulatory Affairs and Quality Assurance ...
    21 CRF0
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    CM&C Technical Writing0
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    Common Technical Dossier0
    Facility AuditsGMP Audits0
    Global Regulatory Affairs0
    Health Sciences Industry0
    IND Annual Reports0
    NDA Annual Report0
    NJ Pharmaceutical Consulting0
    Pre-IND Briefing0
    Pre-NDA Briefing0

    www.bhconsultingservices.com - 2009-02-05
  3. CCDRD AG: Welcome

    CCDRD AG: Full service Clinical Research Organization (CRO)

    www.ccdrdag.com - 2009-02-07
  4. Cato.com

    Cato Research is a full-service contract research and development organization with international resources dedicated to helping pharmaceutical and ...

    www.cato-europe.com - 2009-02-09
  5. Contract Research Organization(CRO), Full Service, with Phase I-II Clinical Research Facility, Phase III-IV Clinical Study Monitoring, Clinical Trial Data ...

    Advanced Biomedical Research, Inc. (ABR) is a scientifically driven, full-service, contract research organization (CRO) providing personalized, technically ...
    Clinicial study report0
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    Phase I-II-III-IV study0
    Prestudy visit0
    Study closeout visit0
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    Study monitoring visit0

    www.abr-pharma.com - 2009-02-04
  6. Concept Heidelberg

    PROGRAMMES GMP and Regulatory Affairs Conferences & Courses in 11 European countries. more IN-HOUSE TRAINING Train your employees on-site – taking into account y ...

    www.concept-heidelberg.com - 2009-02-06
  7. GMP Certification Programme of the European Compliance Academy

    OTHER MEETINGS OF INTEREST ICH Q7 Training Courses 22-26 June 2009, Prague, Czech Republic ICH Q9 Training Course and ICH Q10 and FDA Quality System Training ...

    www.gmp-certification.com - 2009-02-06
  8. Concept Heidelberg: GMP Journals

    PROGRAMMES GMP and Regulatory Affairs Conferences & Courses in 11 European countries. more IN-HOUSE TRAINING Train your employees on-site – taking into account y ...

    www.gmp-journal.com - 2009-02-04
  9. 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
  10. About Global Biopharmaceutical Regulations

    Global Biopharmaceutical Regulations What We Do We specialize in regulatory affairs consulting to the pharmaceutical and related industries for marketing ...
    biologic development0
    drug submission0
    IND applications0
    new drug submission0
    pre-market authorization0

    www.biopharmregulations.com - 2009-02-08

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