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    Name Start Date Credits Format Region Location
    Electronic Submissions: The Next Era of Electronic Submissions Apr 22, 2014 IACET In-Person Instruction North America Horsham, PA, United States
    Key Considerations for the Development and Marketing of Biosimilar Products Apr 24, 2014 IACET In-Person Instruction North America Horsham, PA, United States
    eCTD Submission Apr 25, 2014 In-Person Instruction India Mumbai, MH, India
    2nd Periodic Safety Update Report Information Day Apr 29, 2014 In-Person Instruction Europe London, United Kingdom
    Global Considerations for Regulatory Strategy Development May 05, 2014 IACET In-Person Instruction North America Horsham, PA, United States
    EudraVigilance - Electronic Reporting of ICSRs in the EEA May 05, 2014 In-Person Instruction Europe Vienna, Austria
    TUTORIAL 02: USE OF SOCIAL MEDIA IN RARE DISEASES May 08, 2014 In-Person Instruction Europe Berlin, Germany
    Workshop1: Career Development May 11, 2014 In-Person Instruction China Shanghai, China
    Workshop2: Principles for Successful GXP Inspections: A Hands-On Interactive Approach based on FDA, WHO and Industry Experiences May 11, 2014 In-Person Instruction China Shanghai, China
    Workshop3: Early Clinical Development from First-in-Human (FIH) to Proof of Concept (POC) May 11, 2014 In-Person Instruction China Shanghai, China
    Workshop4: Project Management in Clinical Data Management May 11, 2014 In-Person Instruction China Shanghai, China
    Workshop5: Data Safety Monitoring Board May 11, 2014 In-Person Instruction China Shanghai, China
    Half-day Workshop1: Individual Case Safety Report (ICSR) Medical Review (morning) May 11, 2014 In-Person Instruction China Shanghai, China
    Half-day Workshop2: Good Clinical Data Management Practice Post Trial Data Collection: SAS Programming (afternoon) May 11, 2014 In-Person Instruction China Shanghai, China
    ICH E2B (R3) Individual Case Safety Report (ICSR) Information Day May 13, 2014 In-Person Instruction Europe London, United Kingdom
    Paediatric Investigation Plans (PIP) May 13, 2014 In-Person Instruction Europe London, United Kingdom
    Introduction to Pharmacovigilance and Rules for Expedited Reporting of Individual Case Safety Reports (ICSRs) in Europe May 13, 2014 In-Person Instruction Europe London, United Kingdom
    EU QPPV Pre-Conference Workshop May 13, 2014 In-Person Instruction Europe London, United Kingdom
    EudraVigilance - electronic reporting of ICSRs May 14, 2014 In-Person Instruction Europe London, United Kingdom
    Benefit/Risk Management May 19, 2014 In-Person Instruction Europe Prague, Czech Republic
    EudraVigilance - electronic reporting of ICSRs May 19, 2014 In-Person Instruction Europe London, United Kingdom
    Signal Management in Pharmacovigilance May 21, 2014 In-Person Instruction Europe Prague, Czech Republic
    eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) May 22, 2014 In-Person Instruction Europe London, United Kingdom
    EudraVigilance - Electronic reporting of ICSRs in the EEA Jun 02, 2014 In-Person Instruction Europe Berlin, Germany
    Clinical Project Management Training in Mexico City Jun 05, 2014 In-Person Instruction LATIN AMERICA Mexico City, Mexico
    3rd FDA IND/NDA Training Course in Japan Jun 10, 2014 In-Person Instruction Japan Kyoto, Japan
    #20: Japan Regulatory Environment: Overview of the Organization, Processes, Systems, and Changes Affecting Pharmaceutical Development Jun 15, 2014 IACET In-Person Instruction North America San Diego, CA, United States
    #21: The Sunshine Act: Understanding the Essentials of Compliance Jun 15, 2014 CME, IACET, RN In-Person Instruction North America San Diego, CA, United States
    #22: Preparing for a US FDA Advisory Committee Meeting Jun 15, 2014 IACET In-Person Instruction North America San Diego, CA, United States
    #23: Leadership: How to Organize and Lead People in Group Work Jun 15, 2014 IACET, PMI In-Person Instruction North America San Diego, CA, United States
    #24: Successful Drug Development: Best Practices for Clinical Trial Design, Agency Interactions, and Regulatory Document Writing Jun 15, 2014 IACET In-Person Instruction North America San Diego, CA, United States
    #40: Analysis of Safety Data from Clinical Trials Jun 15, 2014 ACPE, CME, IACET, RN In-Person Instruction North America San Diego, CA, United States
    #41: Quality Oversight of CROs-Clinical Vendors Jun 15, 2014 IACET In-Person Instruction North America San Diego, CA, United States
    #42: Regulatory Affairs for Biologics Jun 15, 2014 IACET In-Person Instruction North America San Diego, CA, United States
    #43: Clinical Statistics for Nonstatisticians Jun 15, 2014 ACPE, CME, IACET, RN In-Person Instruction North America San Diego, CA, United States
    #44: Quality by Design: From Theory to Practice Jun 15, 2014 CME, IACET, RN In-Person Instruction North America San Diego, CA, United States
    #45: Risk Management Plan Jun 15, 2014 ACPE, CME, IACET, RN In-Person Instruction North America San Diego, CA, United States
    #46: The Good Pharmacovigilance Practices In The EU: Lessons Learned and Frequently Asked Implementation Questions Jun 15, 2014 CME, IACET, RN In-Person Instruction North America San Diego, CA, United States
    #30: Influencing Culture, Avoiding Bureaucracy, and Encouraging Innovation Jun 15, 2014 IACET In-Person Instruction North America San Diego, CA, United States
    #31: Large-Scale Regulatory Functional Outsourcing: Emerging Trends, Challenges and Decision Criteria Jun 15, 2014 IACET In-Person Instruction North America San Diego, CA, United States
    #32: Pharmacogenomics and Companion Diagnostics: The Future of Clinical Trials, New Product Development and the Practice of Medicine Jun 15, 2014 ACPE, CME, IACET, RN In-Person Instruction North America San Diego, CA, United States
    #33: Bayesian Evidence Synthesis and Network Meta-analysis Jun 15, 2014 CME, IACET, RN In-Person Instruction North America San Diego, CA, United States
    #34: Preparation of Risk Evaluation and Mitigation Strategies Assessment Reports Jun 15, 2014 ACPE, CME, IACET, RN In-Person Instruction North America San Diego, CA, United States
    #35: Understanding Translational Medicine: Benefits and Innovative Approaches Jun 15, 2014 CME, IACET, RN In-Person Instruction North America San Diego, CA, United States
    Pre-marketing Clinical Safety Jun 16, 2014 In-Person Instruction Europe Amsterdam, Netherlands
    Post-Authorisation Safety Studies (PASS) Jun 18, 2014 In-Person Instruction Europe Amsterdam, Netherlands
    EudraVigilance - electronic reporting of ICSRs Jun 18, 2014 In-Person Instruction Europe London, United Kingdom
    Good Management of Medical Devices: Legal and practical aspects Jun 23, 2014 In-Person Instruction Europe Amsterdam, Netherlands
    Essentials of European Regulatory Affairs Jun 23, 2014 In-Person Instruction Europe Amsterdam, Netherlands
    EudraVigilance - Electronic Reporting of ICSRs in the EEA Jun 23, 2014 In-Person Instruction Europe Basel, Switzerland
    EU Regulation of In-Vitro Diagnostics (IVDs) Jun 26, 2014 In-Person Instruction Europe Amsterdam, Netherlands
    Review a Global Quality Dossier (CTD) with Concept of Quality by Design (QbD) Jul 07, 2014 In-Person Instruction China
    Pragmatic Approaches to Drug Safety Across the Premarketing and Postmarketing Continuum Aug 18, 2014 ACPE, IACET In-Person Instruction North America
    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
    EudraVigilance - electronic reporting of ICSRs Sep 22, 2014 In-Person Instruction Europe Paris, France
    Quality by Design - New Concepts for Chemical and Biotech Product Development and Optimisation Sep 22, 2014 In-Person Instruction Europe Vienna, Austria
    eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) Sep 25, 2014 In-Person Instruction Europe Paris, France
    EudraVigilance - electronic reporting of ICSRs Oct 01, 2014 In-Person Instruction Europe London, United Kingdom
    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 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 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 Oct 20, 2014 In-Person Instruction Europe San Marino, San Marino
    Practical GCP Compliance Auditing of Trials and Systems Oct 22, 2014 In-Person Instruction Europe London, United Kingdom
    Authorisation of Biopharmaceuticals, Biosimilars and Advanced Therapies 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
    Navigating Chemistry, Manufacturing & Controls Through the Drug Development Process Nov 03, 2014 IACET In-Person Instruction North America Horsham, PA, United States
    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 Nov 05, 2014 In-Person Instruction Europe London, United Kingdom
    Electronic Submissions: The Next Era of Electronic Submissions Nov 09, 2014 IACET In-Person Instruction North America Bethesda, MD, United States
    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 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
    Electronic reporting of ICSRs in the EEA Nov 24, 2014 In-Person Instruction Europe Lisboa, Portugal
    EudraVigilance - electronic reporting of ICSRs Dec 03, 2014 In-Person Instruction Europe London, United Kingdom