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    Name Start Date Credits Format Region Location
    EudraVigilance - electronic reporting of ICSRs in the EEA Nov 26, 2014 In-Person Instruction Europe Lisboa, Portugal
    01 - ELECTRONIC TRIAL MASTER FILES (eTMF) - MOVING FROM IMPLEMENTATION TO PROJECT EXCELLENCE Dec 01, 2014 In-Person Instruction Europe Berlin, Germany
    02 - UNDERSTANDING THE IMPACT OF IDENTIFICATION OF MEDICINAL PRODUCTS (IDMP) ON PROCESSES, DATA PROVISION, GOVERNANCE AND IT ARCHITECTURE Dec 01, 2014 In-Person Instruction Europe Berlin, Germany
    EudraVigilance - electronic reporting of ICSRs in the EEA Dec 03, 2014 In-Person Instruction Europe London, United Kingdom
    Joint MHRA/MedDRA Information Day - MedDRA in the Pharmacovigilance Regulatory Process Dec 08, 2014 In-Person Instruction Europe London, United Kingdom
    Preparation of a Successful (CTD) with 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
    Introduction to Pharmacoepidemiology and Applications in Premarketing and Postmarketing Surveillance, Risk Management and Value Demonstration Jan 25, 2015 In-Person Instruction North America Washington, DC, United States
    Pharmacovigilance and Risk Management Planning Jan 25, 2015 In-Person Instruction North America Washington, DC, United States
    PBRERs Jan 25, 2015 In-Person Instruction North America Washington, DC, United States
    Pharmacovigilance System Master File Jan 25, 2015 In-Person Instruction North America Washington, DC, United States
    ICH endorsed PhV training course Feb 12, 2015 In-Person Instruction Europe Algiers, Algeria
    OPDP/APLB and Compliance 101: A Primer Feb 17, 2015 In-Person Instruction North America Washington, DC, United States
    Introduction to Signal Detection and Data Mining Mar 02, 2015 In-Person Instruction North America Washington, DC, United States
    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
    Regulatory Affairs: The IND, NDA, and Postmarketing Mar 15, 2015 In-Person Instruction North America Irvine, CA, United States
    Premarketing Clinical Safety and Pharmacovigilance Mar 23, 2015 In-Person Instruction North America Washington, DC, United States
    Preparing for a FDA Advisory Committee Meeting Apr 01, 2015 In-Person Instruction North America Washington, DC, United States
    01: HOT TOPICS IN PHARMACOVIGILANCE AND ADVERSE REACTION REPORTING Apr 13, 2015 In-Person Instruction Europe Paris, France
    02: INTERACTIONS BETWEEN REGULATORY AND LEGAL IN INTELLECTUAL PROPERTY, PRODUCT LIABILITY AND COMPETITION Apr 13, 2015 In-Person Instruction Europe Paris, France
    03: ANALYSIS OF SAFETY DATA FROM CLINICAL TRIALS Apr 13, 2015 In-Person Instruction Europe Paris, France
    04: PRIVACY AND PERSONAL DATA PROTECTION IN DRUG DEVELOPMENT Apr 13, 2015 In-Person Instruction Europe Paris, France
    07: A LEGAL UPDATE: RECENT AND CURRENT DEVELOPMENTS IN EUROPEAN PHARMACEUTICAL LAW Apr 13, 2015 In-Person Instruction Europe Paris, France
    08: 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
    Global CTD Dossier – Regulatory aspects and focus on quality documentation including concepts of Quality by Design Apr 26, 2015 In-Person Instruction Europe Dakar, Senegal
    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
    Pre-Marketing Clinical Safety May 18, 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
    Diagnosis and Management of Drug-Induced Liver Injury (DILI) Jun 11, 2015 In-Person Instruction Europe Charenton Le Pont, Paris, France
    Pragmatic Approaches to Drug Safety Across the Premarketing and Postmarketing Continuum Aug 10, 2015 In-Person Instruction North America
    Development of a Clinical Study Report Aug 17, 2015 In-Person Instruction North America
    Regulatory Affairs: The IND, NDA, and Postmarketing Aug 17, 2015 In-Person Instruction North America
    Clinical Project Management Aug 24, 2015 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
    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
    Good Management of Medical Devices 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
    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 In-Person Instruction North America
    Regulatory Affairs: The IND, NDA, and Postmarketing Nov 09, 2015 In-Person Instruction North America
    Navigating Chemistry, Manufacturing and Controls Through the Drug Development Process Nov 09, 2015 In-Person Instruction North America
    Advanced Clinical Statistics for NonStatisticians Nov 11, 2015 ACPE, IACET In-Person Instruction North America
    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