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    Name Start Date Credits Format Region Location
    Pragmatic Approaches to Drug Safety Across the Premarketing and Postmarketing Continuum Aug 18, 2014 ACPE, IACET In-Person Instruction North America Boston, MA, United States
    Regulatory Affairs: The IND, NDA, and Postmarketing Aug 18, 2014 IACET In-Person Instruction North America Boston, MA, United States
    Clinical Project Management Aug 18, 2014 IACET, PMI In-Person Instruction North America Boston, MA, United States
    New Drug Product Development and Life Cycle Management Aug 18, 2014 IACET, PMI In-Person Instruction North America Boston, MA, United States
    European Regulatory Affairs: Keeping Your Finger on the Pulse of Marketing Authorizations Aug 18, 2014 IACET In-Person Instruction North America Boston, MA, United States
    Project Risk Management Aug 20, 2014 IACET, PMI In-Person Instruction North America Boston, MA, United States
    Overview of Drug Development Sep 08, 2014 IACET, PMI In-Person Instruction North America Horsham, PA, United States
    Key Considerations for the Development and Marketing of Biosimilar Products Sep 09, 2014 IACET In-Person Instruction North America Horsham, PA, United States
    Development of a Clinical Study Report Sep 15, 2014 IACET In-Person Instruction North America Rockville, MD, United States
    Clinical Statistics for Nonstatisticians Sep 15, 2014 ACPE, IACET In-Person Instruction North America Rockville, MD, United States
    Global Regulatory Strategy and Drug Development in Asia-Pacific, Latin America and Other Emerging Markets Sep 15, 2014 IACET In-Person Instruction North America Rockville, MD, United States
    EudraVigilance - electronic reporting of ICSRs in the EEA Sep 17, 2014 In-Person Instruction Europe Zagreb, Croatia (Hrvatska)
    Medical Approach in Diagnosis and Management of ADRs Sep 22, 2014 In-Person Instruction Europe Charenton Le Pont, Paris, France
    EudraVigilance - electronic reporting of ICSRs in the EEA Sep 22, 2014 In-Person Instruction Europe Paris, France
    Clinical Project Management - Part I Sep 22, 2014 In-Person Instruction Europe Charenton Le Pont, Paris, France
    Quality by Design - New Concepts for Chemical and Biotech Product Development and Optimisation Sep 22, 2014 In-Person Instruction Europe Vienna, Austria
    Diagnosis and Management of Drug-Induced Liver Injury (DILI) Sep 23, 2014 In-Person Instruction Europe Charenton Le Pont, Paris, France
    eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) Sep 25, 2014 In-Person Instruction Europe Paris, France
    EudraVigilance - electronic reporting of ICSRs in the EEA Oct 01, 2014 In-Person Instruction Europe London, United Kingdom
    Pharmacovigilance and Risk Management Planning Oct 01, 2014 ACPE, IACET In-Person Instruction North America
    EudraVigilance - Electronic reporting of ICSRs in the EEA Oct 06, 2014 In-Person Instruction Europe Madrid, Spain
    eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) Oct 09, 2014 In-Person Instruction Europe Madrid, Spain
    EMA Excellence in Pharmacovigilance: Clinical trials and post-marketing Oct 13, 2014 In-Person Instruction Europe London, United Kingdom
    Introduction to Health Technology Assessment (HTA) Oct 13, 2014 In-Person Instruction Europe Charenton Le Pont, Paris, France
    How to prepare for your meeting with Health Authorities Oct 14, 2014 In-Person Instruction Europe Charenton Le Pont, Paris, France
    Introduction to Pharmacovigilance and Rules for Expedited Reporting of Individual Case Safety Reports (ICSRs) in Europe Oct 14, 2014 In-Person Instruction Europe London, United Kingdom
    EudraVigilance - electronic reporting of ICSRs in the EEA Oct 15, 2014 In-Person Instruction Europe London, United Kingdom
    Regulatory Affairs for Biologics Oct 19, 2014 IACET In-Person Instruction North America Irvine, CA, United States
    Postmarketing Drug Safety and Pharmacovigilance Oct 20, 2014 ACPE, IACET In-Person Instruction North America Horsham, PA, United States
    EudraVigilance - electronic reporting of ICSRs in the EEA Oct 20, 2014 In-Person Instruction Europe San Marino, San Marino
    Global CTD Dossier – Regulatory aspects and focus on quality documentation including concepts of Quality by Design Oct 21, 2014 In-Person Instruction Europe Dakar, Senegal
    ICH endorsed PhV training course Oct 21, 2014 In-Person Instruction Europe Dakar, Senegal
    Adaptive Design in Clinical Trials: When and How to Apply Oct 21, 2014 In-Person Instruction North America Philadelphia, PA, United States
    Practical GCP Compliance Auditing of Trials and Systems Oct 22, 2014 In-Person Instruction Europe London, United Kingdom
    Biopharmaceuticals, Biosimilars and Advanced Therapies in Europe - Development and Regulatory Framework in Europe Oct 22, 2014 In-Person Instruction Europe London, United Kingdom
    Clinical Statistics for Non-Statisticians Oct 23, 2014 In-Person Instruction Europe London, United Kingdom
    Biostatistics for Non-Statisticians Oct 27, 2014 In-Person Instruction North America
    Risk Management Plans and Drug Utilization Studies in Canada Oct 27, 2014 In-Person Instruction North America Ottawa, ON, Canada
    Navigating Chemistry, Manufacturing & Controls Through the Drug Development Process Nov 03, 2014 IACET In-Person Instruction North America Horsham, PA, United States
    Advanced Signal Detection - Tools, Triage, Evaluation, and Escalation Nov 03, 2014 IACET In-Person Instruction North America Washington, DC, United States
    Essentials of European Regulatory Affairs Nov 03, 2014 In-Person Instruction Europe Charenton Le Pont, Paris, France
    Signal Management in Pharmacovigilance Nov 03, 2014 In-Person Instruction Europe Charenton Le Pont, Paris, France
    Introduction to Pharmacovigilance and Rules for Expedited Reporting of Individual Case Safety Reports (ICSRs) in Europe Nov 04, 2014 In-Person Instruction Europe London, United Kingdom
    Essentials of Clinical Study Management Nov 05, 2014 In-Person Instruction Europe London, United Kingdom
    US Regulatory Affairs Nov 05, 2014 In-Person Instruction Europe London, United Kingdom
    EudraVigilance - electronic reporting of ICSRs in the EEA Nov 05, 2014 In-Person Instruction Europe London, United Kingdom
    Tutorial 1: From the Pediatric Case Files of FDA Nov 06, 2014 In-Person Instruction North America North Bethesda, MD, United States
    Electronic Submissions: The Next Era of Electronic Submissions Nov 09, 2014 IACET In-Person Instruction North America Bethesda, MD, United States
    Benefit/Risk Management Nov 10, 2014 In-Person Instruction Europe Barcelona, Spain
    Clinical Project Management Part II Nov 10, 2014 In-Person Instruction Europe Barcelona, Spain
    Regulatory Affairs: The IND, NDA, and Postmarketing Nov 10, 2014 IACET In-Person Instruction North America Bethesda, MD, United States
    The Leadership Experience Nov 10, 2014 IACET, PMI In-Person Instruction North America Bethesda, MD, United States
    Risk Management and Safety Communication Strategies Nov 10, 2014 ACPE, IACET In-Person Instruction North America Bethesda, MD, United States
    EudraVigilance - electronic reporting of ICSRs in the EEA Nov 10, 2014 In-Person Instruction Europe Vienna, Austria
    EudraVigilance - electronic reporting of ICSRs in the EEA Nov 17, 2014 In-Person Instruction Europe London, United Kingdom
    eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) Nov 20, 2014 In-Person Instruction Europe London, United Kingdom
    ICH endorsed PhV training course Nov 26, 2014 In-Person Instruction Europe Algiers, Algeria
    EudraVigilance - electronic reporting of ICSRs in the EEA Nov 26, 2014 In-Person Instruction Europe Lisboa, Portugal
    EudraVigilance - electronic reporting of ICSRs in the EEA Dec 03, 2014 In-Person Instruction Europe London, United Kingdom
    Joint MHRA/EMA/MSSO Information Day MedDRA in the Pharmacovigilance Regulatory Process Dec 08, 2014 In-Person Instruction Europe London, United Kingdom
    Review a Global Quality Dossier (CTD) with Concept of Quality by Design (QbD) Dec 08, 2014 In-Person Instruction China
    2nd DIA Advanced Regulatory Affairs Training Course in Japan Dec 08, 2014 In-Person Instruction Japan Tokyo, Japan