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    Name Start Date Credits Format Region Location
    EudraVigilance - electronic reporting of ICSRs in the EEA Jun 3, 2015 In-Person Instruction Europe Berlin, Germany
    2nd DIA European Medicines Regulations and the EU-Network Training Course Jun 4, 2015 In-Person Instruction Japan Tokyo, Japan
    Joint DIA/EMA Information Day on Post-Authorisation Studies (PAS) Jun 5, 2015 In-Person Instruction Europe London, United Kingdom
    EudraVigilance - electronic reporting of ICSRs in the EEA Jun 8, 2015 In-Person Instruction Europe London, United Kingdom
    Medical Approach in Diagnosis and Management of ADRs Jun 10, 2015 In-Person Instruction Europe Paris Montrouge, France
    eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) Jun 11, 2015 In-Person Instruction Europe London, United Kingdom
    Diagnosis and Management of Drug-Induced Liver Injury (DILI) Jun 11, 2015 In-Person Instruction Europe Paris Montrouge, France
    #20: The Sunshine Act: Understanding the Essentials of Compliance Jun 14, 2015 CME, IACET, RN In-Person Instruction North America Washington, DC, United States
    #21: Leadership: How to Organize and Lead People in a Work Group Jun 14, 2015 IACET, PMI In-Person Instruction North America Washington, DC, United States
    #22: Successful Drug Development: Best Practices for Clinical Trial Design, Agency Interactions, and Regulatory Document Writing Jun 14, 2015 IACET In-Person Instruction North America Washington, DC, United States
    #23: How to Prepare for an FDA Inspection Jun 14, 2015 CME, IACET, RN In-Person Instruction North America Washington, DC, United States
    #25: Signal Detection: Identifying and Managing Safety Signals Jun 14, 2015 ACPE, CME, IACET, RN In-Person Instruction North America Washington, DC, United States
    #40: Analysis of Safety Data from Clinical Trials Jun 14, 2015 ACPE, CME, IACET, RN In-Person Instruction North America Washington, DC, United States
    #41: Quality Oversight of CROs-Clinical Vendors Jun 14, 2015 IACET In-Person Instruction North America Washington, DC, United States
    #42: Fundamentals of ANDA Submissions and FDA Expectations Under GDUFA Jun 14, 2015 CME, IACET, RN In-Person Instruction North America Washington, DC, United States
    #43: Clinical Statistics for Nonstatisticians Jun 14, 2015 ACPE, CME, IACET, RN In-Person Instruction North America Washington, DC, United States
    #44: Risk Management and Safety Communication Strategies Jun 14, 2015 ACPE, CME, IACET, RN In-Person Instruction North America Washington, DC, United States
    #45: The Good Pharmacovigilance Practices in the EU: Global Applications Jun 14, 2015 CME, IACET, RN In-Person Instruction North America Washington, DC, United States
    #30: Japan Regulatory Environment: Overview of the Organization, Processes, Systems, and Changes Affecting Pharmaceutical Development Jun 14, 2015 IACET In-Person Instruction North America Washington, DC, United States
    #31: Preparing for a US FDA Advisory Committee Meeting Jun 14, 2015 IACET In-Person Instruction North America Washington, DC, United States
    #32: Influencing Culture, Avoiding Bureaucracy, and Encouraging Innovation Jun 14, 2015 IACET In-Person Instruction North America Washington, DC, United States
    #33: Large-Scale Regulatory Functional Outsourcing: Emerging Trends, Challenges, and Decision Criteria Jun 14, 2015 IACET In-Person Instruction North America Washington, DC, United States
    #34: Preparation of Risk Evaluation and Mitigation Strategies Assessment Reports Jun 14, 2015 ACPE, CME, IACET, RN In-Person Instruction North America Washington, DC, United States
    #35: Ethical Issues in Clinical Trials Jun 14, 2015 CME, IACET, RN In-Person Instruction North America Washington, DC, United States
    Joint EMA/DIA Information Day on ISO IDMP Standards: Achieving Compliance Jun 23, 2015 In-Person Instruction Europe London, United Kingdom
    Joint EMA/DIA Information Day on Risk Management Planning Jun 30, 2015 In-Person Instruction Europe London, United Kingdom
    Global Regulatory Strategy and Drug Development in Asia-Pacific, Latin America, and Other Emerging Markets Aug 3, 2015 In-Person Instruction North America Washington, DC, United States
    Development of a Clinical Study Report Aug 10, 2015 IACET In-Person Instruction North America Boston, MA, United States
    Regulatory Affairs: The IND, NDA, and Postmarketing Aug 10, 2015 IACET In-Person Instruction North America Boston, MA, United States
    Pragmatic Approaches to Drug Safety Across the Premarketing and Postmarketing Continuum Aug 10, 2015 ACPE, IACET In-Person Instruction North America Boston, MA, United States
    European Regulatory Affairs: Keeping Your Finger on the Pulse of Marketing Authorizations Aug 11, 2015 In-Person Instruction North America Boston, MA, United States
    Clinical Project Management Aug 24, 2015 IACET, PMI In-Person Instruction North America Washington, DC, United States
    New Drug Product Development and Life Cycle Management Aug 26, 2015 IACET, PMI In-Person Instruction North America Washington, DC, United States
    Clinical Project Management Part I Sep 16, 2015 In-Person Instruction Europe London, United Kingdom
    Paediatric Investigation Plans (PIP) Sep 17, 2015 In-Person Instruction Europe London, United Kingdom
    Post-Authorisation Safety Studies (PASS) Sep 21, 2015 In-Person Instruction Europe Berlin, Germany
    Medical Devices: Regulation and lifecycle management Sep 21, 2015 In-Person Instruction Europe Vienna, Austria
    Adaptive Design in Clinical Trials: When and How to Apply Sep 21, 2015 IACET In-Person Instruction North America Washington, DC, United States
    Quality by Design - Making next generation process efficiency a reality for Chemical and Biotech Product Development and Optimisation Sep 21, 2015 In-Person Instruction Europe Vienna, Austria
    Joint MHRA/DIA Excellence in Pharmacovigilance Sep 28, 2015 In-Person Instruction Europe London, United Kingdom
    Pragmatic Approaches to Drug Safety Across the Premarketing and Postmarketing Continuum Sep 28, 2015 ACPE, IACET In-Person Instruction North America Toronto, ON, Canada
    Clinical Statistics for Nonstatisticians Sep 28, 2015 ACPE, IACET In-Person Instruction North America Washington, DC, United States
    Introduction to the role of QPPVs Oct 12, 2015 In-Person Instruction Europe London, United Kingdom
    3rd DIA Advanced Regulatory Affairs Training Course in Japan Oct 13, 2015 In-Person Instruction Japan Tokyo, Japan
    Practical GCP Compliance Auditing of Trials and Systems Oct 14, 2015 In-Person Instruction Europe London, United Kingdom
    How to manage a successful health authority interaction Oct 14, 2015 In-Person Instruction Europe London, United Kingdom
    Clinical Statistics for Non-Statisticians Oct 15, 2015 In-Person Instruction Europe London, United Kingdom
    Tutorial 1: Achieving Biosimilarity Through Matching of Critical Quality Attributes to Reference Product’s Oct 18, 2015 In-Person Instruction North America Bethesda, MD, United States
    Risk Management and Safety Communication Oct 26, 2015 ACPE, IACET In-Person Instruction North America Washington, DC, United States
    Benefit/Risk Management Nov 3, 2015 In-Person Instruction Europe Paris Montrouge, France
    Essentials and Overview of the Regulatory Framework in Europe Nov 4, 2015 In-Person Instruction Europe Paris Montrouge, France
    Signal Management in Pharmacovigilance Nov 5, 2015 In-Person Instruction Europe Paris Montrouge, France
    Postmarketing Drug Safety & Pharmacovigilance Nov 9, 2015 ACPE, IACET In-Person Instruction North America Philadelphia, PA, United States
    Building the eCTD - Practical solutions to compiling electronic submissions Nov 9, 2015 In-Person Instruction Europe Dubai, United Arab Emirates
    Regulatory Affairs: The IND, NDA, and Postmarketing Nov 9, 2015 IACET In-Person Instruction North America Philadelphia, PA, United States
    Navigating Chemistry, Manufacturing and Controls Through the Drug Development Process Nov 9, 2015 IACET In-Person Instruction North America Philadelphia, PA, United States
    Advanced Clinical Statistics for NonStatisticians Nov 11, 2015 ACPE, IACET In-Person Instruction North America Philadelphia, PA, United States
    US Regulatory Affairs: A Comprehensive Review of Regulatory Procedures for INDs and NDAs in the US Nov 16, 2015 In-Person Instruction Europe London, United Kingdom
    Clinical Project Management Part II Nov 16, 2015 In-Person Instruction Europe London, United Kingdom
    Biopharmaceuticals, Biosimilars and Advanced Therapies in Europe - Development and Regulatory Framework Nov 25, 2015 In-Person Instruction Europe Vienna, Austria