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Pharmanalytical Consulting, Inc. is committed to the success of our customers in emerging, start-up and resource-limited pharmaceutical companies. Our ...
chemical manufacturing control  contract resource organization 
www.pharmanalytical.com - 2009-02-09
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B&H Consulting Services, Inc. is committed to assisting health sciences companies effectively meet their global Regulatory Affairs and Quality Assurance ...
21 CRF  CM&C  CM&C Technical Writing  CMC Technical Writing  Common Technical Dossier  Facility AuditsGMP Audits  Global Regulatory Affairs  Health Sciences Industry  IND Annual Reports  NDA Annual Report  NJ Pharmaceutical Consulting  Pre-IND Briefing  Pre-NDA Briefing 
www.bhconsultingservices.com - 2009-02-05
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CCDRD AG: Full service Clinical Research Organization (CRO)
www.ccdrdag.com - 2009-02-07
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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
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Advanced Biomedical Research, Inc. (ABR) is a scientifically driven, full-service, contract research organization (CRO) providing personalized, technically ...
Clinicial study report  Investigative site  Phase I-II-III-IV study  Prestudy visit  Study closeout visit  Study initiation visit  Study monitoring visit 
www.abr-pharma.com - 2009-02-04
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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
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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
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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
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HORN Pharmaceutical Consulting provides regulatory and business advice to companies from the pharmaceutical, biotechnology and medical device industries.
Biologic License Application  CMC-documents  European MAA  quality overall summaries 
www.horn-pharma.de - 2009-02-13
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Global Biopharmaceutical Regulations What We Do We specialize in regulatory affairs consulting to the pharmaceutical and related industries for marketing ...
biologic development  drug submission  IND applications  new drug submission  pre-market authorization 
www.biopharmregulations.com - 2009-02-08
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