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Harmonisation
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951	N° 72 – décembre[removed]Harmonisation des régimes invalidité-décès des artisans et des commerçants Le Régime social des indépendants couvre le risque Add to Reading List Source URL: www.rsi.fr Language: French - Date: 2013-10-14 03:09:06
952	Guidance for Industry E2B(M): Data Elements for Transmission of Individual Case Safety Reports: Questions and Answers Add to Reading List Source URL: www.fda.gov Language: English Clinical research Pharmaceutical industry Drug safety Pharmaceuticals policy Food and Drug Administration Clinical trial International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Pharmaceutical sciences Pharmacology Research
953	Guidance for Industry E2C Clinical Safety Data Management: Periodic Safety Update Reports for Marketed Drugs Add to Reading List Source URL: www.fda.gov Language: English Medicine Pharmaceuticals policy Clinical research Drug safety Pharmaceutical industry Pharmacovigilance Regulatory requirement Food and Drug Administration International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Pharmaceutical sciences Pharmacology Health
954	Guidance for Industry E16 Biomarkers Related to Drug or Biotechnology Product Development: Context, Structure, and Format of Qualification Add to Reading List Source URL: www.fda.gov Language: English Clinical research Pharmacology Drug discovery Pharmaceutical industry Clinical Data Management Biomarker Electronic Common Technical Document Proteomics International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Medicine Biology Research
955	Microsoft Word - 9621fnl.doc Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical industry Clinical research Pharmaceuticals policy Food and Drug Administration Quality Validation International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Center for Biologics Evaluation and Research Good manufacturing practice Medicine Health Pharmaceutical sciences
956	Microsoft Word - 9391fnl.doc Add to Reading List Source URL: www.fda.gov Language: English Food and Drug Administration Clinical research Pharmaceuticals policy Drug safety United States Public Health Service International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Center for Biologics Evaluation and Research Pharmacopoeia Capillary electrophoresis Medicine Health Pharmaceutical sciences
957	Microsoft Word - 8671fnl.DOC Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences Pharmacology Clinical research Pharmacopoeias Pharmaceuticals policy International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Center for Biologics Evaluation and Research Biologic Center for Drug Evaluation and Research Food and Drug Administration Medicine Health
958	Guidance for Industry Q1C Stability Testing for New Dosage Forms ICH November 1996 Add to Reading List Source URL: www.fda.gov Language: English Food and Drug Administration Dosage forms Clinical research Drug safety Center for Biologics Evaluation and Research Biologic International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Center for Drug Evaluation and Research Tablet Pharmaceutical sciences Pharmacology Medicine
959	Microsoft Word - 9116fnl.doc Add to Reading List Source URL: www.fda.gov Language: English Food and Drug Administration Clinical research Pharmaceuticals policy Drug safety Therapeutics International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Center for Biologics Evaluation and Research Pharmacopoeia Health Canada Medicine Health Pharmaceutical sciences
960	Guidance for Industry M4S: August 2001 ICH Add to Reading List Source URL: www.fda.gov Language: English Clinical Data Management Food and Drug Administration Pharmacology Common Technical Document International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Clinical trial Electronic Common Technical Document Center for Biologics Evaluation and Research Research Clinical research Medicine