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    Name Start Date Credits Format Region Location
    Clinical Investigator: Module 2 - Conducting The Study Jul 25, 2014 ACPE, CME Online Instruction North America Online
    Clinical Investigator: Module 1 - Study Preparation and Initiation Jul 25, 2014 ACPE, CME Online Instruction North America Online
    Informed Consent Jul 25, 2014 ACPE Online Instruction North America Online
    Crisis Management Jul 25, 2014 ACPE, IACET Online Instruction North America Online
    Database Management Jul 25, 2014 ACPE, IACET Online Instruction North America Online
    Literature Evaluation Jul 25, 2014 ACPE, IACET Online Instruction North America Online
    Literature Searching Jul 25, 2014 ACPE, IACET Online Instruction North America Online
    Medical Inquiries Jul 25, 2014 ACPE, IACET Online Instruction North America Online
    Medical Writing Jul 25, 2014 IACET Online Instruction North America Online
    Product Labeling Jul 25, 2014 ACPE, IACET Online Instruction North America Online
    Regulatory Issues Jul 25, 2014 ACPE, IACET Online Instruction North America Online
    Statistics for Medical Communications Professionals Jul 25, 2014 ACPE, IACET Online Instruction North America Online
    The Use of Mobile Medical Applications as Companions Jul 25, 2014 Online Instruction Global Online
    Regulating a Social World Jul 25, 2014 Online Instruction Global Online
    Generic Drug Labeling Proposed Rule and Safety Updates Jul 25, 2014 Online Instruction Global Online
    English Literacy and Spanish Transcreation of Patient Documents: Concepts for Low Literacy Materials Jul 25, 2014 Online Instruction Global Online
    Big Data: Impact of Health Care Reform on Collaborations and Strategies Jul 25, 2014 Online Instruction Global Online
    Implementation of the FDASIA Patient Provisions Jul 25, 2014 Online Instruction Global Online
    Complimentary: Regulatory and Real World Evidence Challenges of Rare Diseases and Orphan Drugs Jul 25, 2014 Online Instruction Global Online
    Variations in the European Union: CMC/Quality Changes Jul 25, 2014 Online Instruction Global Online
    Good Pharmacovigilance Practice: How Good has it Proven to be for Industry? Jul 25, 2014 Online Instruction Global Online
    Safety and Social Media: Is this the Question or the Answer Jul 25, 2014 Online Instruction Global Online
    Pharmacovigilance and Risk Management: Patient Perspective Jul 25, 2014 Online Instruction Global Online
    Complimentary Patient-Centeredness and Engagement in Clinical Research: Opportunities for Industry Jul 25, 2014 Online Instruction Global Online
    Drug Safety Regulatory Requirements Jul 25, 2014 ACPE, IACET Online Instruction Global Online
    Premarketing Clinical Trial Safety Jul 25, 2014 ACPE, IACET Online Instruction Global Online
    Postmarketing Safety Management Jul 25, 2014 Online Instruction Global Online
    Basics of Signal Detection and Pharmacoepidemiology Jul 25, 2014 Online Instruction Global Online
    Safety Audits and Inspections Jul 25, 2014 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 1: Fundamentals of Clinical Pharmacology: Pharmacokinetics Jul 25, 2014 Online Instruction Global Online
    Designed for Success: Utilizing Protocol Quality by Design (QbD) to Plan Clinical Studies Jul 25, 2014 Online Instruction Global Online
    Negotiation and Influence Jul 25, 2014 Online Instruction Global Online
    China Update: Regulatory Changes and Implications Jul 25, 2014 Online Instruction Global Online
    Evaluation and Management of Cardiac Conditions in Oncology Patients Jul 25, 2014 Online Instruction Global Online
    Risk Management of Medicinal Products: REMS and RMP - Need for Harmonization Within the ICH Region? Jul 25, 2014 Online Instruction Global Online
    Introduction to Drug Safety Jul 25, 2014 ACPE, IACET Online Instruction Global Online
    How to Prepare for a Safety Inspection Jul 25, 2014 Online Instruction Global Online
    CDER Town Meeting: Safety Hot Topics Jul 25, 2014 Online Instruction Global Online
    Assessing the Benefits and Risks of Medicines: Webinar Series - Part 1: Introduction to the Benefit-Risk - Why is Everyone Talking about Benefit-Risk? Jul 25, 2014 Online Instruction Global Online
    Assessing the Benefits and Risks of Medicines: Webinar Series Part 2 - Benefit-Risk Assessment a Changing Regulatory Landscape Jul 25, 2014 Online Instruction Global Online
    Assessing the Benefits and Risks of Medicines: Webinar Series - Part 3: Framing for Benefit-Risk Assessment and Communication Jul 25, 2014 Online Instruction Global Online
    Assessing the Benefits and Risks of Medicines: Webinar Series - Part 4: Clinical Judgment and Pragmatic Considerations for Endpoint Selection and Display in Benefit-Risk Jul 25, 2014 Online Instruction Global Online
    Assessing the Benefits and Risks of Medicines: Webinar Series- Part 5: Stated Choice Methods for Valuing Benefits and Risks Jul 25, 2014 Online Instruction Global Online
    Assessing the Benefits and Risks of Medicines: Webinar Series-Part 6: Multi-criteria Decision Analysis to Assist in the Decision Making Process Jul 25, 2014 Online Instruction Global Online
    Assessing the Benefits and Risks of Medicines: Webinar Series- Part 7: A Structured, Quantitative Health Outcomes Approach to Drug Benefit-Risk Analysis Jul 25, 2014 Online Instruction Global Online
    Assessing the Benefits and Risks of Medicines: Webinar Series- Part 8: Visualization and Communication of Benefit-Risk Jul 25, 2014 Online Instruction Global Online
    New Good Pharmacovigilance Practice (GVP) Documents in Canada Jul 25, 2014 Online Instruction Global Online
    Clinical Statistics for Nonstatisticians Jul 25, 2014 Online Instruction Global Online
    Development of a Clinical Study Report Jul 25, 2014 Online Instruction Global Online
    Complimentary Biomarker Strategies for More Efficient Early-Phase Drug Development in Alzheimer's Disease Jul 25, 2014 Online Instruction Global Online
    CardioVascular Safety: The New Paradigm - Proarrhythmic Assessment of New Drugs without the Thorough QT Study Jul 25, 2014 Online Instruction Global Online
    CardioVascular Safety – What are the Key Issues Regarding Blood Pressure Assessment During Clinical Development Jul 25, 2014 Online Instruction Global Online
    Introductory Principles and Application of Risk Management within Clinical Operations Jul 25, 2014 Online Instruction Global Online
    Electronic Submissions 101 – Essential MS Word and Adobe Acrobat Tools/Skills and Current IT Options Jul 25, 2014 Online Instruction Global Online
    A Tour of FDA Jul 25, 2014 Online Instruction Global Online
    A Tour of Health Canada Jul 25, 2014 Online Instruction Global Online
    A Tour of Health Europe Jul 25, 2014 Online Instruction Global Online
    Aspects of Regulatory History Jul 25, 2014 Online Instruction Global Online
    Bioresearch Monitoring Program (BIMO): Introduction Jul 25, 2014 Online Instruction Global Online
    The Clinical Development Process: Investigational Product, Plan, and Data Management Jul 25, 2014 Online Instruction Global Online
    Drug Safety & Adverse Event Reporting Jul 25, 2014 Online Instruction Global Online
    Ethical Review Boards Jul 25, 2014 Online Instruction Global Online
    Ethics as the Foundation to Clinical Research Jul 25, 2014 Online Instruction Global Online
    Awareness of FDA Inspections for Pharmaceutical Manufacturers Jul 25, 2014 Online Instruction Global Online
    Biotechnology: An Overview of Compliance Considerations Jul 25, 2014 Online Instruction Global Online
    Change Control Jul 25, 2014 Online Instruction Global Online
    Clinical Trial Audits and Consequences of Non-Compliance Jul 25, 2014 Online Instruction Global Online
    Computerized Systems Inspections in the Medical Device Industry Jul 25, 2014 Online Instruction Global Online
    European Union Clinical Trials Directive Jul 25, 2014 Online Instruction Global Online
    GMP Principals of SOPs Jul 25, 2014 Online Instruction Global Online
    GMP Updates - Enforcement Changes at the New FDA Jul 25, 2014 Online Instruction Global Online
    GMPs for API Bulk Manufacturers Jul 25, 2014 Online Instruction Global Online
    Good Clinical Practices (GCPs) for New Product Investigations Jul 25, 2014 Online Instruction Global Online
    Good Laboratory Practices (GLPs) Jul 25, 2014 Online Instruction Global Online
    GxPs Jul 25, 2014 Online Instruction Global Online
    HIPAA - The Impact on Clinical Research Jul 25, 2014 Online Instruction Global Online
    Introduction to GMPs Jul 25, 2014 Online Instruction Global Online
    Investigational Product Development Jul 25, 2014 Online Instruction Global Online
    ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials Jul 25, 2014 Online Instruction Global Online
    Key Concepts of Process Validation Jul 25, 2014 Online Instruction Global Online
    Laboratory Specimens for Clinical Research Jul 25, 2014 Online Instruction Global Online
    Medical Device Safety Reporting Jul 25, 2014 Online Instruction Global Online
    Orientation to GMP Compliance Jul 25, 2014 Online Instruction Global Online
    Overview of the Clinical Research Process Jul 25, 2014 Online Instruction Global Online
    Part 11: Electronic Records and Signatures - Application Jul 25, 2014 Online Instruction Global Online
    Part 11: Electronic Records; Electronic Signatures Jul 25, 2014 Online Instruction Global Online
    Principles of Good Documentation Jul 25, 2014 Online Instruction Global Online
    Protection of Human Subjects in Clinical Trials Jul 25, 2014 Online Instruction Global Online
    Selecting and Managing Clinical Contract Research Organizations (CROs) Jul 25, 2014 Online Instruction Global Online
    Understanding Post-Approval Changes Jul 25, 2014 Online Instruction Global Online
    Computerized Systems Inspections in the Pharmaceutical Industry Jul 25, 2014 Online Instruction Global Online
    Basics of the PhRMA Code Jul 25, 2014 Online Instruction Global Online
    Basics of AdvaMed Code Jul 25, 2014 Online Instruction Global Online
    Eucomed Guidelines on Interactions with Healthcare Professionals Jul 25, 2014 Online Instruction Global Online
    Introduction to Medical Device Health Care Compliance Jul 25, 2014 Online Instruction Global Online
    Foreign Corrupt Practices Act Jul 25, 2014 Online Instruction Global Online
    Global Anti-bribery Jul 25, 2014 Online Instruction Global Online
    Variations to Marketing Authorisation in Europe Jul 25, 2014 Online Instruction Global Online
    Registration of Monoclonal Antibodies Jul 25, 2014 Online Instruction Global Online
    How to Gain Approval to Market a Generic Medicinal Product in the USA Jul 25, 2014 Online Instruction Global Online
    Pharmacokinetics and Pharmacodynamics in Drug Registration Jul 25, 2014 Online Instruction Global Online
    Measurement in Clinical Trials: An Examination of the FDA Position on Review of Clinical Outcome Assessments (COAs) Jul 25, 2014 Online Instruction Global Online
    The Electronic Trial Master File: So Much More than Just a Secure Document Repository Jul 25, 2014 Online Instruction Global Online
    Planning and Implementing Large Cardiovascular Outcomes Studies: Opportunities & Challenges Jul 25, 2014 Online Instruction Global Online
    Press the Easy Button – Ensure Consistency and Compliance for your Documents through Automation Jul 25, 2014 Online Instruction Global Online
    When Outsourcing Stops Making Sense Jul 25, 2014 Online Instruction Global Online
    Complimentary Quintiles/DIA Webinar - Giving Your Study The Right Start Toward Success Through Optimal Country and Site Selection Jul 25, 2014 Online Instruction Global Online
    Complimentary - Risk-Based Monitoring: Regulatory Expectation and Operational Application Jul 25, 2014 Online Instruction Global Online
    Fundamentals of Project Management for Nonproject Managers Jul 25, 2014 Online Instruction Global Online
    Planning and Managing Your Project Jul 25, 2014 Online Instruction Global Online
    Change Management, Issues Management, Escalation Management Jul 25, 2014 Online Instruction Global Online
    Project Risk Management: Dealing with the Certainty of Uncertainty Jul 25, 2014 Online Instruction Global Online
    Team Building and Development Jul 25, 2014 Online Instruction Global Online
    Preparing a Clinical Trial Budget Jul 25, 2014 Online Instruction Global Online
    Introduction to the European Union Institutions and Regulatory Authority Jul 25, 2014 Online Instruction Global Online
    Introduction to US Institutions and Regulatory Authority (FDA) Jul 25, 2014 Online Instruction Global Online
    Introduction to Japanese Institutions and Regulatory Authorities Jul 25, 2014 Online Instruction Global Online
    Overview of the CTD and eCTD Jul 25, 2014 Online Instruction Global Online
    Introduction to the International Conference on Harmonisation (ICH) Jul 25, 2014 Online Instruction Global Online
    The Regulatory Development of a Drug Jul 25, 2014 Online Instruction Global Online
    Basics of Clinical Trials Jul 25, 2014 Online Instruction Global Online
    How to Register Medicinal Products through the Centralized Procedure Jul 25, 2014 Online Instruction Global Online
    How to Register Medicinal Products through the Mutual Recognition Procedure Jul 25, 2014 Online Instruction Global Online
    How to Maintain Marketing Approvals in Europe for Centrally Authorised Products Jul 25, 2014 Online Instruction Global Online
    How to Register a New Drug in the USA Jul 25, 2014 Online Instruction Global Online
    How to Register Medicinal Products through the Decentralized Procedure Jul 25, 2014 Online Instruction Global Online
    Access to Unapproved Drugs through Compassionate Use Jul 25, 2014 Online Instruction Global Online
    Regulatory Requirements for the Conduct of Clinical Trials in Europe Jul 25, 2014 Online Instruction Global Online
    Orphan Drugs in the USA, European Union, and Japan Jul 25, 2014 Online Instruction Global Online
    Regulatory Requirements for the Submission of Investigational New Drug Applications in the USA (INDs) Jul 25, 2014 Online Instruction Global Online
    Meeting Opportunities with Regulatory Agencies Jul 25, 2014 Online Instruction Global Online
    A Regulatory Perspective of Biosimilars in Emerging Markets Jul 25, 2014 Online Instruction Global Online
    Combination Products and Convergence: An Overview of Clinical Benefits, Regulatory Issues & Manufacturing Challenges Jul 25, 2014 Online Instruction Global Online
    Strategies for Successfully Introducing REMS to Your Organization: From Development and Implementation and Internal and External Evaluation Jul 25, 2014 Online Instruction Global Online
    The Case of the New England Compounding Center: Learning from the Tragedy Jul 25, 2014 Online Instruction Global Online
    Complimentary - From the Clinic to the CFO: Adaptive Trials and Financial Decision-Making Jul 25, 2014 Online Instruction Global Online
    Complimentary - The Affiliate Challenge – How to Improve Compliance and Efficiency when Working with Regional Affiliates Jul 25, 2014 Online Instruction Global Online
    The Future of Personalized Medicine and Companion Diagnostics Jul 25, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 1: Overall Challenge: The Vision of Better Medicines for Children Jul 25, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part III: Regulatory Framework EU Jul 25, 2014 Online Instruction Global Online
    Seven-Part Pediatric Drug Development Webinar Series - Part IV: Dosing in Children Jul 25, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part II Regulatory Framework US Overview Jul 25, 2014 Online Instruction Global Online
    Basics of the IND Jul 25, 2014 Online Instruction Global Online
    Basics of the NDA Jul 25, 2014 Online Instruction Global Online
    Regulatory Aspects of Prescription Drug/Biologics Advertising and Promotional Labeling Jul 25, 2014 Online Instruction Global Online
    The Current State of Quality Oversight (QO) in the Pharmaceutical Industry Jul 25, 2014 Online Instruction Global Online
    Supplements and Other Changes to an Approved Application Jul 25, 2014 Online Instruction Global Online
    Planning and Managing Your Projects Jul 29, 2014 IACET, PMI Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 2: Fundamentals of Clinical Pharmacology: Pharmacodynamics Aug 07, 2014 ACPE, IACET Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part V: Technical Development: Pediatric Formulations Aug 12, 2014 ACPE, IACET Online Instruction Global Online
    Team Building and Development Aug 13, 2014 IACET, PMI Online Instruction Global Online
    Pragmatic Approaches to Drug Safety Across the Premarketing and Postmarketing Continuum Aug 18, 2014 ACPE, IACET In-Person Instruction North America Boston, MA, United States
    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
    Five-Part Series on Fundamentals of Clinical Pharmacology For Drug Development - Part 3: Principles of Modeling and Simulation Sep 04, 2014 ACPE, IACET Online Instruction Global Online
    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
    Clinical Trials Transparency 3-Part Series: Moving the Debate Forward - Realizing the Benefits of Providing Greater Access to Clinical Trial Data: Part 1 - Paving the Way for Greater Access To Data Sep 09, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part VI: Preclinical Toxicology & Safety Sep 09, 2014 ACPE, IACET Online Instruction Global Online
    Art of Writing a Clinical Overview Sep 09, 2014 IACET Online Instruction Global Online
    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
    Global Regulatory Strategy and Drug Development in Asia-Pacific, Latin America and Other Emerging Markets Sep 15, 2014 IACET In-Person Instruction North America Rockville, MD, United States
    EudraVigilance - electronic reporting of ICSRs in the EEA Sep 17, 2014 In-Person Instruction Europe Zagreb, Croatia (Hrvatska)
    DIA Biosimilars 2014 Sep 18, 2014 ACPE, IACET Meetings North America Washington, DC, United States
    Improving Efficiency Within the Current Regulatory System: Results of the Escher project Sep 18, 2014 Meetings Europe Brussels, Belgium
    Medical Approach in Diagnosis and Management of ADRs Sep 22, 2014 In-Person Instruction Europe Charenton Le Pont, Paris, France
    EDM and ERS 2014 Sep 22, 2014 Meetings North America Washington, DC, United States
    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
    8th Annual European Medical Information and Communications Conference Sep 23, 2014 Meetings Europe London, United Kingdom
    Clinical Trials Workshop I - Translating the New Clinical Trials Regulation into Practice Sep 23, 2014 Meetings Europe London, United Kingdom
    Strategies for Good Clinical Practice Audits Sep 23, 2014 IACET, RN Online Instruction Global Online
    Diagnosis and Management of Drug-Induced Liver Injury (DILI) Sep 23, 2014 In-Person Instruction Europe Charenton Le Pont, Paris, France
    Clinical Trials Workshop II - Translating the New Transparency Requirements into Practice Sep 24, 2014 Meetings Europe London, United Kingdom
    Workshop on Biorelevant in-vitro Performance Testing of Orally Administered Dosage Forms Jointly organised by FIP and DIA Sep 24, 2014 Meetings Europe Amsterdam, Netherlands
    11th Latin American Conference of Clinical Research Sep 25, 2014 Meetings LATIN AMERICA Monterrey, Mexico
    eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) Sep 25, 2014 In-Person Instruction Europe Paris, France
    Introduction to Signal Detection and Data Mining Sep 29, 2014 IACET Online Instruction Global Online
    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
    DIA Canadian Pharmacovigilance & Risk Management Oct 02, 2014 IACET Meetings North America
    EudraVigilance - Electronic reporting of ICSRs in the EEA Oct 06, 2014 In-Person Instruction Europe Madrid, Spain
    Joint DIA/ICOS Cardio-Oncology Conference Oct 09, 2014 Meetings Europe Prague, Czech Republic
    eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) Oct 09, 2014 In-Person Instruction Europe Madrid, Spain
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 4: Determining the Safe First Human Dose Oct 09, 2014 ACPE, IACET Online Instruction Global Online
    EMA Excellence in Pharmacovigilance: Clinical trials and post-marketing Oct 13, 2014 In-Person Instruction Europe London, United Kingdom
    Introduction to Health Technology Assessment (HTA) Oct 13, 2014 In-Person Instruction Europe Charenton Le Pont, Paris, France
    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
    Seven-Part Series on Pediatric Drug Development - Part VII: Operational Challenges of Pediatric Clinical Trials Oct 14, 2014 ACPE, IACET Online Instruction Global Online
    EudraVigilance - electronic reporting of ICSRs in the EEA Oct 15, 2014 In-Person Instruction Europe London, United Kingdom
    DIA 2014 9th Annual India Conference: The Future of Indian Health Care: Patients, Access and Innovation Oct 16, 2014 Meetings India Mumbai, India
    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
    ICH endorsed PhV training course Oct 21, 2014 In-Person Instruction Europe Dakar, Senegal
    Adaptive Design in Clinical Trials: When and How to Apply Oct 21, 2014 In-Person Instruction North America Philadelphia, PA, United States
    Clinical Trials Transparency 3-Part Series: Moving the Debate Forward - Realizing the Benefits of Providing Greater Access to Clinical Trial Data: Part 2 - Connecting the Research Community: Data Sharing – Perspectives from Academia and Patient Advocacy Oct 21, 2014 Online Instruction Global Online
    4th African Regulatory Conference (ARC) Oct 22, 2014 Meetings Europe Dakar, Senegal
    Practical GCP Compliance Auditing of Trials and Systems Oct 22, 2014 In-Person Instruction Europe London, United Kingdom
    Biopharmaceuticals, Biosimilars and Advanced Therapies in Europe - 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
    5th DIA Cardiac Safety Workshop in Japan Oct 23, 2014 Meetings Japan Tokyo, Japan
    Risk Management Plans and Drug Utilization Studies in Canada Oct 27, 2014 In-Person Instruction North America Ottawa, ON, Canada
    DIA’s Annual Canadian Meeting: Thinking Globally, Acting Locally for The Well-Being of the Patient Oct 28, 2014 Meetings North America Ottawa, ON, Canada
    Patient Engagement throughout the Full Spectrum of Drug Development: An Interactive Workshop for Life Science Companies and Patient Groups Oct 29, 2014 Meetings North America Washington, DC, United States
    DIA Meeting on Combination Products Oct 29, 2014 IACET Meetings North America Washington, DC, United States
    DIA Meeting on Companion Diagnostics Oct 30, 2014 IACET Meetings North America Washington, DC, United States
    Negotiation and Influence Oct 30, 2014 IACET, PMI Online Instruction Global Online
    Advanced Signal Detection - Tools, Triage, Evaluation, and Escalation Nov 03, 2014 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
    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
    ISPE/DIA Workshop on Computer Systems Compliance “Maintain Data Integrity to Reduce Risk for the Patient” Nov 06, 2014 Meetings Europe Basel, Switzerland
    Tutorial 1: From the Pediatric Case Files of FDA Nov 06, 2014 In-Person Instruction North America North Bethesda, MD, United States
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 5: Assessment of QT Prolongation Nov 06, 2014 ACPE, IACET Online Instruction Global Online
    Pediatric Research Conference 2014: Transforming the Pediatric Research Landscape through Innovation and Forward Thinking Nov 06, 2014 Meetings 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
    Joint DIA/AEMPS Statistics Workshop Nov 10, 2014 Meetings Europe Barcelona, Spain
    EudraVigilance - electronic reporting of ICSRs in the EEA Nov 10, 2014 In-Person Instruction Europe Vienna, Austria
    Clinical Trials Transparency 3-Part Series: Part 3 - Understanding the Legislation Landscape: Regulatory Updates from the FDA and EMA Nov 12, 2014 Online Instruction Global Online
    11th Annual Meeting DIA Japan 2014 Nov 16, 2014 Meetings 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
    1st Maghreb Regulatory Conference Nov 24, 2014 Meetings Europe Algiers, Algeria
    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
    15th Annual Conference on Electronic Document Management (eDM) Dec 02, 2014 Meetings Europe Berlin, Germany
    Biosimilars Conference Dec 02, 2014 Meetings Europe Berlin, Germany
    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
    Review a Global Quality Dossier (CTD) with Concept of 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
    Pharmacovigilance and Risk Management Strategies 2015 Jan 26, 2015 Meetings North America Washington, DC, United States
    CMC Workshop 2015 Apr 13, 2015 Meetings North America Washington, DC, United States
    8th Annual Clinical Forum Apr 13, 2015 Meetings Europe Paris, France
    27th Annual EuroMeeting Apr 13, 2015 Meetings Europe Paris, France
    DIA 2015 51st Annual Meeting Jun 14, 2015 Meetings North America Washington, DC, United States