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    Name Start Date Credits Format Region Location
    Introduction to Pharmacoepidemiology and Applications in Premarketing and Postmarketing Surveillance, Risk Management and Value Demonstration Jan 25, 2015 IACET, RN In-Person Instruction North America Washington, DC, United States
    Pharmacovigilance and Risk Management Planning Jan 25, 2015 ACPE, IACET, RN In-Person Instruction North America Washington, DC, United States
    PBRERs Jan 25, 2015 IACET, RN In-Person Instruction North America Washington, DC, United States
    Pharmacovigilance System Master File Jan 25, 2015 IACET, RN In-Person Instruction North America Washington, DC, United States
    EudraVigilance - electronic reporting of ICSRs in the EEA Jan 28, 2015 In-Person Instruction Europe London, United Kingdom
    Excellence in Pharmacovigilance: Clinical Trials and Post-Marketing Feb 09, 2015 In-Person Instruction Europe London, United Kingdom
    Bayesian Methods for Drug Safety Evaluation and Signal Detection Feb 10, 2015 IACET In-Person Instruction North America Arlington, VA, United States
    Use of Historical Data in Clinical Trials Feb 10, 2015 IACET In-Person Instruction North America Arlington, VA, United States
    ICH endorsed PhV training course Feb 12, 2015 In-Person Instruction Europe Algiers, Algeria
    EudraVigilance - electronic reporting of ICSRs in the EEA Feb 16, 2015 In-Person Instruction Europe London, United Kingdom
    OPDP/APLB and Compliance 101: A Primer Feb 17, 2015 ACPE, IACET In-Person Instruction North America Washington, DC, United States
    eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) Feb 19, 2015 In-Person Instruction Europe London, United Kingdom
    Introduction to Signal Detection and Data Mining Mar 02, 2015 IACET In-Person Instruction North America Washington, DC, United States
    eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) Mar 02, 2015 In-Person Instruction Europe Madrid, Spain
    EudraVigilance - electronic reporting of ICSRs in the EEA Mar 04, 2015 In-Person Instruction Europe Madrid, Spain
    Benefit/Risk Management Mar 10, 2015 In-Person Instruction Europe Hamburg, Germany
    Essentials of European Regulatory Affairs Mar 10, 2015 In-Person Instruction Europe Hamburg, Germany
    Introduction to Pharmacovigilance and Rules for Expedited Reporting of Individual Case Safety Reports (ICSRs) in Europe Mar 10, 2015 In-Person Instruction Europe London, United Kingdom
    EudraVigilance - electronic reporting of ICSRs in the EEA Mar 11, 2015 In-Person Instruction Europe London, United Kingdom
    Regulatory Affairs: The IND, NDA, and Postmarketing Mar 15, 2015 In-Person Instruction North America Irvine, CA, United States
    Core Curriculum Mar 15, 2015 In-Person Instruction North America Glendale, AZ, United States
    Medical Communications: Compliance in 2015 Mar 16, 2015 In-Person Instruction North America
    EudraVigilance - electronic reporting of ICSRs in the EEA Mar 16, 2015 In-Person Instruction Europe Vienna, Austria
    eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) Mar 19, 2015 In-Person Instruction Europe Vienna, Austria
    Premarketing Clinical Safety and Pharmacovigilance Mar 23, 2015 IACET In-Person Instruction North America Washington, DC, United States
    EudraVigilance - Electronic Reporting of ICSRs in the EEA Mar 25, 2015 In-Person Instruction Europe Bucharest, Romania
    Preparing for a FDA Advisory Committee Meeting Mar 30, 2015 IACET In-Person Instruction North America Washington, DC, United States
    EM01: HOT TOPICS IN PHARMACOVIGILANCE AND ADVERSE REACTION REPORTING Apr 13, 2015 In-Person Instruction Europe Paris, France
    EM02: INTERACTIONS BETWEEN REGULATORY AND LEGAL IN INTELLECTUAL PROPERTY, PRODUCT LIABILITY AND COMPETITION Apr 13, 2015 In-Person Instruction Europe Paris, France
    EM03: ANALYSIS OF SAFETY DATA FROM CLINICAL TRIALS Apr 13, 2015 In-Person Instruction Europe Paris, France
    EM04: PRIVACY AND PERSONAL DATA PROTECTION IN DRUG DEVELOPMENT Apr 13, 2015 In-Person Instruction Europe Paris, France
    EM05: MOVING FROM RISK MANAGEMENT TO BENEFIT/RISK MANAGEMENT EMBEDDING PHARMACOVIGILANCE PRINCIPLES INTO THE PRODUCT LIFE CYCLE Apr 13, 2015 In-Person Instruction Europe Paris, France
    EM06: MODELLING AND SIMULATION Apr 13, 2015 In-Person Instruction Europe Paris, France
    CF01: A LEGAL UPDATE: RECENT AND CURRENT DEVELOPMENTS IN EUROPEAN PHARMACEUTICAL LAW Apr 13, 2015 In-Person Instruction Europe Paris, France
    CF02: ENSURING DATA QUALITY AND DETECTING POTENTIAL FRAUD/GCP MISCONDUCT Apr 13, 2015 In-Person Instruction Europe Paris, France
    Regulatory Affairs for Biologics Apr 14, 2015 In-Person Instruction North America Bethesda, MD, United States
    EudraVigilance - electronic reporting of ICSRs in the EEA Apr 15, 2015 In-Person Instruction Europe Paris, France
    Advanced Signal Detection - Tools, Triage, Evaluation, and Escalation Apr 20, 2015 In-Person Instruction North America Washington, DC, United States
    EudraVigilance - electronic reporting of ICSRs in the EEA Apr 20, 2015 In-Person Instruction Europe London, United Kingdom
    eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) Apr 23, 2015 In-Person Instruction Europe London, United Kingdom
    ICH endorsed PhV training course Apr 26, 2015 In-Person Instruction Europe Dakar, Senegal
    Key Considerations for the Development and Marketing of Biosimilar Products Apr 27, 2015 In-Person Instruction North America Washington, DC, United States
    Signal Management in Pharmacovigilance Apr 27, 2015 In-Person Instruction Europe Basel, Switzerland
    How to prepare for Pharmacovigilance Audits and Inspections Apr 28, 2015 In-Person Instruction Europe Basel, Switzerland
    Pragmatic Approaches to Drug Safety Across the Premarketing and Postmarketing Continuum Apr 29, 2015 ACPE, IACET In-Person Instruction North America Washington, DC, United States
    EudraVigilance - electronic reporting of ICSRs in the EEA May 04, 2015 In-Person Instruction Europe San Marino, San Marino
    Introduction to Health Technology Assessment (HTA) May 06, 2015 In-Person Instruction Europe Amsterdam, Netherlands
    Electronic Submissions: The Next Era of Electronic Submissions May 14, 2015 IACET In-Person Instruction North America Philadelphia, PA, United States
    Essentials of Clinical Study Management May 18, 2015 In-Person Instruction Europe London, United Kingdom
    Pre-Marketing Clinical Safety May 18, 2015 In-Person Instruction Europe London, United Kingdom
    Introduction to Pharmacovigilance and Rules for Expedited Reporting of Individual Case Safety Reports (ICSRs) in Europe May 19, 2015 In-Person Instruction Europe London, United Kingdom
    EudraVigilance - electronic reporting of ICSRs in the EEA May 20, 2015 In-Person Instruction Europe London, United Kingdom
    EudraVigilance - electronic reporting of ICSRs in the EEA Jun 03, 2015 In-Person Instruction Europe Berlin, Germany
    EudraVigilance - electronic reporting of ICSRs in the EEA Jun 08, 2015 In-Person Instruction Europe London, United Kingdom
    Medical Approach in Diagnosis and Management of ADRs Jun 10, 2015 In-Person Instruction Europe Charenton Le Pont, Paris, 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 Charenton Le Pont, Paris, 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
    #24: Pharmacogenomics and Companion Diagnostics: The Future of Clinical Trials, New Product Development and the Practice of Medicine 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 Pharmacovigiliance 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
    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
    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 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 In-Person Instruction North America Washington, DC, United States
    Adaptive Design in Clinical Trials: When and How to Apply Sep 15, 2015 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
    Quality by Design - New Concepts for Chemical and Biotech Product Development and Optimisation Sep 21, 2015 In-Person Instruction Europe Vienna, Austria
    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
    Practical GCP Compliance Auditing of Trials and Systems Oct 14, 2015 In-Person Instruction Europe London, United Kingdom
    How to Prepare for Your Meeting with Health Authorities and Present Your Product 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
    Risk Management and Safety Communication Oct 26, 2015 In-Person Instruction North America Washington, DC, United States
    Benefit/Risk Management Nov 03, 2015 In-Person Instruction Europe Charenton Le Pont, Paris, France
    Signal Management in Pharmacovigilance Nov 05, 2015 In-Person Instruction Europe Charenton Le Pont, Paris, France
    Postmarketing Drug Safety & Pharmacovigilance Nov 09, 2015 ACPE, IACET In-Person Instruction North America Philadelphia, PA, United States
    Regulatory Affairs: The IND, NDA, and Postmarketing Nov 09, 2015 In-Person Instruction North America Philadelphia, PA, United States
    Navigating Chemistry, Manufacturing and Controls Through the Drug Development Process Nov 09, 2015 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 - Development and Regulatory Framework in Europe Nov 25, 2015 In-Person Instruction Europe Vienna, Austria
    Essentials of European Regulatory Affairs Nov 26, 2015 In-Person Instruction Europe Vienna, Austria