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    Name Start Date Credits Format Region Location
    EudraVigilance - electronic reporting of ICSRs in the EEA Sep 17, 2014 In-Person Instruction Europe Zagreb, Croatia (Hrvatska)
    Clinical Project Management (Basic-Int) Sep 18, 2014 In-Person Instruction China Suzhou, China
    Regulatory Information Management (RIM) Sep 21, 2014 IACET In-Person Instruction North America Washington, DC, United States
    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 Toronto, ON, Canada
    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
    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
    Adaptive Design in Clinical Trials: When and How to Apply Oct 21, 2014 IACET 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 - 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
    4th DIA Project Management Training Course in Japan Oct 27, 2014 PMI In-Person Instruction Japan Tokyo, Japan
    Biostatistics for Non-Statisticians Oct 27, 2014 IACET In-Person Instruction North America
    Risk Management Plans and Drug Utilization Studies in Canada Oct 27, 2014 IACET In-Person Instruction North America Ottawa, ON, Canada
    Combination Products: A Comprehensive Overview of Premarket Opportunities and Postmarket Challenges! Oct 28, 2014 IACET In-Person Instruction North America Washington, DC, United States
    Navigating Chemistry, Manufacturing & Controls Through the Drug Development Process Nov 03, 2014 IACET In-Person Instruction North America Horsham, PA, United States
    How to Prepare for Pharmacovigilance Audits and Inspections Nov 03, 2014 In-Person Instruction Europe Charenton Le Pont, Paris, France
    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
    From the Pediatric Case Files of FDA Nov 06, 2014 IACET 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
    #1 Basic Introduction for Non-Specialist: Drug-Drug Interaction and Summary of Change in New Japanese Drug-Drug Interaction Guideline Nov 16, 2014 In-Person Instruction Japan Tokyo, Japan
    #2 Next Steps for Content of Company Core Data Sheet Prepared by Western Companies - Part 1 Nov 16, 2014 In-Person Instruction Japan Tokyo, Japan
    #3 Action Learning for Six Sigma Analytical Tools Using Real Case Studies Nov 16, 2014 In-Person Instruction Japan Tokyo, Japan
    #4 Coaching as a Diverse Communication Tool Across Functions and Areas Nov 16, 2014 In-Person Instruction Japan Tokyo, Japan
    #5 The Basics of “Investigator Initiated Trial (IIT)” Regulation Nov 16, 2014 In-Person Instruction Japan Tokyo, Japan
    #6 Prediction for Human Pharmacokinetics and Safety Using Systems Pharmacology Nov 16, 2014 In-Person Instruction Japan Tokyo, Japan
    #7 Next Steps for Content of Company Core Data Sheet Prepared by Western Companies - Part 2 Nov 16, 2014 In-Person Instruction Japan Tokyo, Japan
    #8 An Introduction to Adaptive Designs Nov 16, 2014 In-Person Instruction Japan Tokyo, Japan
    #9 Let’s Learn and Talk about Project Management Basics of the Clinical Study in Medical Institutes! Nov 16, 2014 In-Person Instruction Japan Tokyo, Japan
    #10 HTA 2016? What are the challenges for Japan? Nov 16, 2014 In-Person Instruction Japan Tokyo, Japan
    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
    Tutorial 01:ELECTRONIC TRIAL MASTER FILES (eTMF) - MOVING FROM IMPLEMENTATION TO PROJECT EXCELLENCE Dec 01, 2014 In-Person Instruction Europe Berlin, Germany
    Tutorial 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
    The Basics of Clinical Data Management From Start to End Dec 03, 2014 IACET In-Person Instruction North America Washington, DC, United States
    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
    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
    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