DIA
Drug Information Association Logo

Advanced Search

MM-DD-YYYY

Add Filter

    Advanced Search

    Find Meetings & Training 

    Name Start Date Credits Format Region Location
    EudraVigilance - electronic reporting of ICSRs in the EEA Mar 04, 2015 In-Person Instruction Europe Madrid, Spain
    Clinical Investigator: Module 2 - Conducting the Study Mar 06, 2015 ACPE, CME Online Instruction North America Online
    Clinical Investigator: Module 1 - Study Preparation and Initiation Mar 06, 2015 ACPE, CME Online Instruction North America Online
    Informed Consent Mar 06, 2015 ACPE Online Instruction North America Online
    Crisis Management Mar 06, 2015 ACPE, IACET Online Instruction North America Online
    Database Management Mar 06, 2015 ACPE, IACET Online Instruction North America Online
    Literature Evaluation Mar 06, 2015 ACPE, IACET Online Instruction North America Online
    Literature Searching Mar 06, 2015 ACPE, IACET Online Instruction North America Online
    Medical Inquiries Mar 06, 2015 ACPE, IACET Online Instruction North America Online
    Medical Writing Mar 06, 2015 IACET Online Instruction North America Online
    Product Labeling Mar 06, 2015 ACPE, IACET Online Instruction North America Online
    Regulatory Issues Mar 06, 2015 ACPE, IACET Online Instruction North America Online
    Statistics for Medical Communications Professionals Mar 06, 2015 ACPE, IACET Online Instruction North America Online
    Novel Data Sources: The Positive Impact of Social Media and Online Networks for Engaging with Patients Mar 06, 2015 Online Instruction Global Online
    US Advertising & Promotion Requirements for Promotional Regulatory Compliance: Fundamentals for Marketing Drugs and Devices Mar 06, 2015 Online Instruction Global Online
    US Digital Requirements for Promotional Regulatory Compliance: Fundamentals for Marketing Drugs and Devices Mar 06, 2015 Online Instruction Global Online
    European Advertising & Promotion Requirements for Regulatory Compliance: Comparing Fundamentals for Marketing Drugs in 5 Major European Markets (United Kingdom, Italy, Spain, France, and Germany) Mar 06, 2015 Online Instruction Global Online
    Generic Drug Labeling Proposed Rule and Safety Updates Mar 06, 2015 Online Instruction Global Online
    Target Product Profile – Strategies to Optimize Drug Development, Product Labeling, and Commercialization Mar 06, 2015 Online Instruction Global Online
    GVP Module IX Compliant Signal Management Systems in Pharmacovigilance: A Tale of Two Experiences Mar 06, 2015 Online Instruction Global Online
    The Role of the Clinical Data Manager Mar 06, 2015 Online Instruction Global Online
    Implementation of the FDASIA Patient Provisions Mar 06, 2015 Online Instruction Global Online
    Complimentary: Regulatory and Real World Evidence Challenges of Rare Diseases and Orphan Drugs Mar 06, 2015 Online Instruction Global Online
    Variations in the European Union: CMC/Quality Changes Mar 06, 2015 Online Instruction Global Online
    Proarrhythmia Mar 06, 2015 Online Instruction Global Online
    Facets of Drug-Induced Kidney Injury and Regulatory Perspective Mar 06, 2015 Online Instruction Global Online
    Impact on Drug Development of Novel Translational Safety Biomarkers for Improved Detection of Drug-Induced Acute Kidney Injury Mar 06, 2015 Online Instruction Global Online
    Pharmacovigilance and Risk Management: Patient Perspective Mar 06, 2015 Online Instruction Global Online
    Drug Safety Regulatory Requirements Mar 06, 2015 ACPE, IACET Online Instruction Global Online
    Premarketing Clinical Trial Safety Mar 06, 2015 ACPE, IACET Online Instruction Global Online
    Postmarketing Safety Management Mar 06, 2015 ACPE, IACET Online Instruction Global Online
    Basics of Signal Detection and Pharmacoepidemiology Mar 06, 2015 ACPE, IACET Online Instruction Global Online
    Safety Audits and Inspections Mar 06, 2015 ACPE, IACET Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 1: Fundamentals of Clinical Pharmacology: Pharmacokinetics Mar 06, 2015 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 2: Fundamentals of Clinical Pharmacology: Pharmacodynamics Mar 06, 2015 Online Instruction Global Online
    Pharmacovigilance and Global Harmonization Updates Mar 06, 2015 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology For Drug Development - Part 3: Principles of Modeling and Simulation Mar 06, 2015 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 4: Determining the Safe First Human Dose Mar 06, 2015 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 5: Assessment of QT Prolongation Mar 06, 2015 Online Instruction Global Online
    Designed for Success: Utilizing Protocol Quality by Design (QbD) to Plan Clinical Studies Mar 06, 2015 Online Instruction Global Online
    Negotiation and Influence Mar 06, 2015 Online Instruction Global Online
    Introduction to Drug Safety Mar 06, 2015 ACPE, IACET Online Instruction Global Online
    How to Prepare for a Safety Inspection Mar 06, 2015 Online Instruction Global Online
    Implementation and Status of Periodic Benefit-Risk Evaluation Reporting (PBRER) in Canada Mar 06, 2015 Online Instruction Global Online
    Clinical Statistics for Nonstatisticians Mar 06, 2015 Online Instruction Global Online
    Advanced Clinical Statistics for Nonstatisticians Mar 06, 2015 Online Instruction Global Online
    Development of a Clinical Study Report Mar 06, 2015 Online Instruction Global Online
    Art of Writing a Clinical Overview Mar 06, 2015 Online Instruction Global Online
    Introductory Principles and Application of Risk Management within Clinical Operations Mar 06, 2015 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 6: Preclinical Toxicology & Safety Mar 06, 2015 Online Instruction Global Online
    Complimentary - Need to Reinvent the Clinical Trial? Innovate, Collaborate & Integrate Mar 06, 2015 Online Instruction Global Online
    Disruptive Innovation in Medical Information Mar 06, 2015 Online Instruction Global Online
    A Tour of FDA Mar 06, 2015 Online Instruction Global Online
    A Tour of Health Canada Mar 06, 2015 Online Instruction Global Online
    A Tour of Health Europe Mar 06, 2015 Online Instruction Global Online
    Aspects of Regulatory History Mar 06, 2015 Online Instruction Global Online
    Bioresearch Monitoring Program (BIMO): Introduction Mar 06, 2015 Online Instruction Global Online
    The Clinical Development Process: Investigational Product, Plan, and Data Management Mar 06, 2015 Online Instruction Global Online
    Ethical Review Boards Mar 06, 2015 Online Instruction Global Online
    Ethics as the Foundation to Clinical Research Mar 06, 2015 Online Instruction Global Online
    Awareness of FDA Inspections for Pharmaceutical Manufacturers Mar 06, 2015 Online Instruction Global Online
    Biotechnology: An Overview of Compliance Considerations Mar 06, 2015 Online Instruction Global Online
    Change Control Mar 06, 2015 Online Instruction Global Online
    Clinical Trial Audits and Consequences of Non-Compliance Mar 06, 2015 Online Instruction Global Online
    Computerized Systems Inspections in the Medical Device Industry Mar 06, 2015 Online Instruction Global Online
    European Union Clinical Trials Directive Mar 06, 2015 Online Instruction Global Online
    GMP Principals of SOPs Mar 06, 2015 Online Instruction Global Online
    GMP Updates - Enforcement Changes at the New FDA Mar 06, 2015 Online Instruction Global Online
    GMPs for API Bulk Manufacturers Mar 06, 2015 Online Instruction Global Online
    Good Clinical Practices (GCPs) for New Product Investigations Mar 06, 2015 Online Instruction Global Online
    Good Laboratory Practices (GLPs) Mar 06, 2015 Online Instruction Global Online
    GxPs Mar 06, 2015 Online Instruction Global Online
    HIPAA - The Impact on Clinical Research Mar 06, 2015 Online Instruction Global Online
    Introduction to GMPs Mar 06, 2015 Online Instruction Global Online
    Investigational Product Development Mar 06, 2015 Online Instruction Global Online
    ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials Mar 06, 2015 Online Instruction Global Online
    Key Concepts of Process Validation Mar 06, 2015 Online Instruction Global Online
    Laboratory Specimens for Clinical Research Mar 06, 2015 Online Instruction Global Online
    Medical Device Safety Reporting Mar 06, 2015 Online Instruction Global Online
    Orientation to GMP Compliance Mar 06, 2015 Online Instruction Global Online
    Overview of the Clinical Research Process Mar 06, 2015 Online Instruction Global Online
    Part 11: Electronic Records and Signatures - Application Mar 06, 2015 Online Instruction Global Online
    Part 11: Electronic Records; Electronic Signatures Mar 06, 2015 Online Instruction Global Online
    Principles of Good Documentation Mar 06, 2015 Online Instruction Global Online
    Protection of Human Subjects in Clinical Trials Mar 06, 2015 Online Instruction Global Online
    Selecting and Managing Clinical Contract Research Organizations (CROs) Mar 06, 2015 Online Instruction Global Online
    Understanding Post-Approval Changes Mar 06, 2015 Online Instruction Global Online
    Computerized Systems Inspections in the Pharmaceutical Industry Mar 06, 2015 Online Instruction Global Online
    Basics of the PhRMA Code Mar 06, 2015 Online Instruction Global Online
    Basics of AdvaMed Code Mar 06, 2015 Online Instruction Global Online
    Eucomed Guidelines on Interactions with Healthcare Professionals Mar 06, 2015 Online Instruction Global Online
    Introduction to Medical Device Health Care Compliance Mar 06, 2015 Online Instruction Global Online
    Foreign Corrupt Practices Act Mar 06, 2015 Online Instruction Global Online
    Global Anti-bribery Mar 06, 2015 Online Instruction Global Online
    Variations to Marketing Authorisation in Europe Mar 06, 2015 Online Instruction Global Online
    Registration of Monoclonal Antibodies Mar 06, 2015 Online Instruction Global Online
    How to Gain Approval to Market a Generic Medicinal Product in the USA Mar 06, 2015 Online Instruction Global Online
    Pharmacokinetics and Pharmacodynamics in Drug Registration Mar 06, 2015 Online Instruction Global Online
    Complimentary Quintiles/DIA Webinar - Giving Your Study The Right Start Toward Success Through Optimal Country and Site Selection Mar 06, 2015 Online Instruction Global Online
    Implementing Risk-Based Monitoring: Practical Approaches Mar 06, 2015 Online Instruction Global Online
    Complimentary - Innovative Strategies for Developing Safer Cancer Therapies Mar 06, 2015 Online Instruction Global Online
    Complimentary - Risk-Based Monitoring: Regulatory Expectation and Operational Application Mar 06, 2015 Online Instruction Global Online
    Fundamentals of Project Management for Nonproject Managers Mar 06, 2015 Online Instruction Global Online
    Planning and Managing Your Projects Mar 06, 2015 Online Instruction Global Online
    Team Building and Development Mar 06, 2015 Online Instruction Global Online
    Introduction to the European Union Institutions and Regulatory Authority Mar 06, 2015 Online Instruction Global Online
    Introduction to US Institutions and Regulatory Authority (FDA) Mar 06, 2015 Online Instruction Global Online
    Introduction to Japanese Institutions and Regulatory Authorities Mar 06, 2015 Online Instruction Global Online
    Overview of the CTD and eCTD Mar 06, 2015 Online Instruction Global Online
    Introduction to the International Conference on Harmonisation (ICH) Mar 06, 2015 Online Instruction Global Online
    The Regulatory Development of a Drug Mar 06, 2015 Online Instruction Global Online
    Basics of Clinical Trials Mar 06, 2015 Online Instruction Global Online
    How to Register Medicinal Products through the Centralized Procedure Mar 06, 2015 Online Instruction Global Online
    How to Register Medicinal Products through the Mutual Recognition Procedure Mar 06, 2015 Online Instruction Global Online
    How to Maintain Marketing Approvals in Europe for Centrally Authorised Products Mar 06, 2015 Online Instruction Global Online
    How to Register a New Drug in the USA Mar 06, 2015 Online Instruction Global Online
    How to Register Medicinal Products through the Decentralized Procedure Mar 06, 2015 Online Instruction Global Online
    Access to Unapproved Drugs through Compassionate Use Mar 06, 2015 Online Instruction Global Online
    Regulatory Requirements for the Conduct of Clinical Trials in Europe Mar 06, 2015 Online Instruction Global Online
    Orphan Drugs in the USA, European Union, and Japan Mar 06, 2015 Online Instruction Global Online
    Regulatory Requirements for the Submission of Investigational New Drug Applications in the USA (INDs) Mar 06, 2015 Online Instruction Global Online
    Meeting Opportunities with Regulatory Agencies Mar 06, 2015 Online Instruction Global Online
    Complementary - How New Electronic Trial Master File (eTMF) Data Standards Can Enhance Clinical Trial Efficiency and Quality Mar 06, 2015 Online Instruction Global Online
    Complimentary - Regulatory Solutions in the Cloud - 10 Questions You Can't Afford NOT to Ask Mar 06, 2015 Online Instruction Global Online
    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 Mar 06, 2015 Online Instruction Global Online
    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 Groups Mar 06, 2015 Online Instruction Global Online
    Complimentary - From the Clinic to the CFO: Adaptive Trials and Financial Decision-Making Mar 06, 2015 Online Instruction Global Online
    Adverse Event Reporting Requirements: IND and Postmarketing Mar 06, 2015 Online Instruction Global Online
    Complimentary - The Affiliate Challenge – How to Improve Compliance and Efficiency when Working with Regional Affiliates Mar 06, 2015 Online Instruction Global Online
    The Future of Personalized Medicine and Companion Diagnostics Mar 06, 2015 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 1: Overall Challenge: The Vision of Better Medicines for Children Mar 06, 2015 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 3: Regulatory Framework EU Mar 06, 2015 Online Instruction Global Online
    Seven-Part Pediatric Drug Development Webinar Series - Part 4: Dosing in Children Mar 06, 2015 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 2: Regulatory Framework US Overview Mar 06, 2015 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 5: Technical Development: Pediatric Formulations Mar 06, 2015 Online Instruction Global Online
    Basics of the IND Mar 06, 2015 Online Instruction Global Online
    Basics of the NDA Mar 06, 2015 Online Instruction Global Online
    Regulatory Aspects of Prescription Drug/Biologics Advertising and Promotional Labeling Mar 06, 2015 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 7: Operational Challenges of Pediatric Clinical Trials Mar 06, 2015 Online Instruction Global Online
    Supplements and Other Changes to an Approved Application Mar 06, 2015 Online Instruction Global Online
    Clinical Trials Transparency 3 Part Webinar Series - Part 3: Understanding the Legislation Landscape: Regulatory Updates from the FDA, EMA and Health Canada Mar 06, 2015 Online Instruction Global Online
    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
    Preparing a Clinical Trial Budget Mar 10, 2015 IACET, PMI Online Instruction Global Online
    EudraVigilance - electronic reporting of ICSRs in the EEA Mar 11, 2015 In-Person Instruction Europe London, United Kingdom
    3rd DIA Clinical Operation & Monitoring Workshop in Japan Mar 12, 2015 Meetings Japan Tokyo, Japan
    Complimentary Webinar - How to Cut Clinical Trial Timelines in Half Mar 12, 2015 Online Instruction Global Online
    Expert Reactor Panel: IOM Report on Sharing Clinical Trial Data Mar 13, 2015 Online Instruction Global Online
    Regulatory Affairs: The IND, NDA, and Postmarketing Mar 15, 2015 IACET In-Person Instruction North America Irvine, CA, United States
    Core Curriculum Mar 15, 2015 ACPE, IACET, RN In-Person Instruction North America Glendale, AZ, United States
    AMWA Workshop - Fundamentals of Ethics and Practical Applications (RR) [4020] Mar 15, 2015 IACET, RN In-Person Instruction North America
    Medical Communications: Compliance in 2015 Mar 16, 2015 ACPE, IACET, RN In-Person Instruction North America
    Medical Science Liaison Tutorial – The Basics for Success Mar 16, 2015 IACET, RN In-Person Instruction North America
    AMWA Workshop – Reporting Correlation and Regression Analyses (RR/G/SG) [4011] Mar 16, 2015 ACPE, IACET, RN In-Person Instruction North America
    EudraVigilance - electronic reporting of ICSRs in the EEA Mar 16, 2015 In-Person Instruction Europe Vienna, Austria
    Medical & Scientific Communications 2015 Annual Forum Mar 16, 2015 ACPE, IACET, RN Meetings North America Glendale, AZ, United States
    2nd DIA Risk Management Workshop in Japan Mar 19, 2015 Meetings Japan Tokyo, Japan
    ICH endorsed PhV training course Mar 23, 2015 In-Person Instruction Europe Rabat, Morocco
    Premarketing Clinical Safety and Pharmacovigilance Mar 23, 2015 IACET In-Person Instruction North America Washington, DC, United States
    Clinical Data Validation Workshop Mar 25, 2015 Meetings China
    1st Maghreb Regulatory Conference Mar 25, 2015 Meetings Europe Rabat, Morocco
    EudraVigilance - Electronic Reporting of ICSRs in the EEA Mar 25, 2015 In-Person Instruction Europe Bucharest, Romania
    Preparing for a US FDA Advisory Committee Meeting Mar 30, 2015 IACET In-Person Instruction North America Washington, DC, United States
    GVP Module IX Compliant Signal Management Systems in Pharmacovigilance: A Tale of Two Experiences Apr 02, 2015 ACPE, IACET Online Instruction Global Online
    Complimentary Webinar - How Revolutionary Machine Learning Advancements Improve Healthcare Research Productivity, Reduce Complexity, and Drive Discovery of Valuable Insights and Relationships across Disparate Content Repositories Apr 08, 2015 Online Instruction Global Online
    CMC Workshop 2015 Apr 13, 2015 ACPE, IACET Meetings North America Bethesda, MD, United States
    Information Day on ICH Apr 13, 2015 Meetings Europe Paris, France
    8th Annual Clinical Forum Apr 13, 2015 Meetings Europe Paris, France
    27th Annual EuroMeeting Apr 13, 2015 Meetings Europe Paris, France
    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 (M&S) / MODEL INFORMED DRUG DISCOVERY AND DVELEOPMENT (MID3) 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 IACET 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
    Tutorial 1: Statisticians as Leaders Apr 19, 2015 IACET In-Person Instruction North America North Bethesda, MD, United States
    Tutorial 2: Propensity Score Methodology Application to Observational Comparative Studies in Regulatory Settings Apr 19, 2015 IACET In-Person Instruction North America North Bethesda, MD, United States
    Tutorial 3: Subgroup Analysis in Clinical Trials Apr 19, 2015 IACET In-Person Instruction North America North Bethesda, MD, United States
    Tutorial 4: Dose Finding in Drug Development: Methods and Implementation Apr 19, 2015 IACET In-Person Instruction North America North Bethesda, MD, United States
    Advanced Signal Detection - Tools, Triage, Evaluation, and Escalation Apr 20, 2015 In-Person Instruction North America Washington, DC, United States
    DIA/FDA Statistics 2015 Forum Apr 20, 2015 IACET Meetings North America North Bethesda, MD, United States
    EudraVigilance - electronic reporting of ICSRs in the EEA Apr 20, 2015 In-Person Instruction Europe London, United Kingdom
    9th DIA Annual Conference in Japan for Asian New Drug Development Apr 20, 2015 Meetings Japan Tokyo, Japan
    eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) Apr 23, 2015 In-Person Instruction Europe London, United Kingdom
    4th DIA FDA IND/NDA Training Course Apr 23, 2015 In-Person Instruction Japan Tokyo, Japan
    ICH endorsed PhV training course Apr 26, 2015 In-Person Instruction Europe Dakar, Senegal
    4th African Regulatory Conference Apr 27, 2015 Meetings Europe Dakar, Senegal
    Biosimilar Development: Strategies and Regulatory Requirements for Global Market Entry Apr 27, 2015 IACET In-Person Instruction North America Washington, DC, United States
    Key Considerations for Biosimilar R&D Workshop Apr 27, 2015 Meetings China
    Signal Management in Pharmacovigilance Apr 27, 2015 In-Person Instruction Europe Basel, Switzerland
    Information Day on New Services and Systems in Pharmacovigilance Apr 28, 2015 In-Person Instruction Europe London, United Kingdom
    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
    Individual Case Safety Report (ICSR) Information Day Apr 29, 2015 In-Person Instruction Europe London, United Kingdom
    EudraVigilance - electronic reporting of ICSRs in the EEA May 04, 2015 In-Person Instruction Europe San Marino, San Marino
    Basics of the IND Phase May 04, 2015 IACET Online Instruction Global Online
    Oversight of Clinical Monitoring: Trends and Strategies May 05, 2015 IACET Online Instruction Global Online
    HTA for Non-HTA user May 06, 2015 In-Person Instruction Europe Amsterdam, Netherlands
    eRegulatory and Intelligence Annual Conference May 11, 2015 Meetings North America Philadelphia, PA, United States
    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
    Drug-Induced Cardiotoxicity Conference May 18, 2015 Meetings Europe Basel, Switzerland
    5th DIA Project Management Training Course in Japan May 18, 2015 In-Person Instruction Japan Kyoto, Japan
    Basics of the NDA Phase May 18, 2015 IACET Online Instruction Global Online
    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
    DIA Canadian Pharmacovigilance & Risk Management Meeting May 21, 2015 Meetings North America Toronto, ON, Canada
    1st DIA Risk Management & Safety Communication Strategies Training Course in Japan May 21, 2015 In-Person Instruction Japan Tokyo, Japan
    The 7th DIA China Annual Meeting May 24, 2015 Meetings China Shanghai, China
    How to Prepare for a Safety Inspection Jun 01, 2015 IACET Online Instruction Global Online
    EudraVigilance - electronic reporting of ICSRs in the EEA Jun 03, 2015 In-Person Instruction Europe Berlin, Germany
    2nd DIA European Medicines Regulations and the EU-Network Training Course Jun 04, 2015 In-Person Instruction Japan Tokyo, Japan
    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 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
    #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
    #25: Signal Detection: Identifying and Managing Safety Signals Jun 14, 2015 ACPE, CME, IACET, RN In-Person Instruction North America Washington, DC, United States
    DIA 2015 51st Annual Meeting: Develop. Innovate. Advance. Jun 14, 2015 Meetings 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
    4th Global Animal Health Conference 2015: regulatory convergence Jun 24, 2015 Meetings Europe Dar Es Salaam, Tanzania, United Republic of
    DIA-TOPRA Workshop on Adaptive Pathways Jun 30, 2015 Meetings Europe Brussels, Belgium
    Adverse Event Reporting Requirements: IND and Post-marketing Jul 13, 2015 Online Instruction Global Online
    Interactions with the FDA during IND/NDA Phases Jul 16, 2015 Online Instruction Global Online
    Global Regulatory Strategy and Drug Development in Asia-Pacific, Latin America and Other Emerging Markets Aug 03, 2015 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 IACET 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
    Overview of Drug Development in Japan Sep 02, 2015 Online Instruction Global Online
    DIA/FDA Oligonucleotide-based Therapeutic Conference 2015 Sep 09, 2015 Meetings North America Washington, DC, United States
    DIA/FDA Oligonucleotide-Based Therapeutics Conference Call for Posters Sep 09, 2015 Meetings North America Washington, DC, United States
    Adaptive Design in Clinical Trials: When and How to Apply Sep 14, 2015 IACET In-Person Instruction North America Washington, DC, United States
    Clinical Project Management Part I Sep 16, 2015 In-Person Instruction Europe London, United Kingdom
    Patient Engagement in Benefit-Risk Assessment throughout the Life Cycle of Medical Products Sep 17, 2015 Meetings North America North Bethesda, MD, 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
    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
    The New Medical Device Regulation Information Day Sep 22, 2015 Meetings Europe Vienna, Austria
    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 Signal Detection and Data Mining Oct 05, 2015 IACET Online Instruction Global Online
    Introduction to the role of QPPVs Oct 12, 2015 In-Person Instruction Europe
    9th European Forum for Qualified Person for Pharmacovigilance (QPPV) and Pre-Conference Workshop Oct 13, 2015 Meetings Europe London, United Kingdom
    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 ACPE, IACET In-Person Instruction North America Washington, DC, United States
    Benefit/Risk Management Nov 03, 2015 In-Person Instruction Europe Paris Montrouge, France
    Essentials of European Regulatory Affairs Nov 04, 2015 In-Person Instruction Europe Paris Montrouge, France
    Signal Management in Pharmacovigilance Nov 05, 2015 In-Person Instruction Europe Paris Montrouge, France
    Postmarketing Drug Safety & Pharmacovigilance Nov 09, 2015 ACPE, IACET In-Person Instruction North America Philadelphia, PA, United States
    Building the eCTD - Practical solutions to compiling electronic submissions Nov 09, 2015 In-Person Instruction Europe Dubai, United Arab Emirates
    Regulatory Affairs: The IND, NDA, and Postmarketing Nov 09, 2015 IACET In-Person Instruction North America Philadelphia, PA, United States
    Navigating Chemistry, Manufacturing and Controls Through the Drug Development Process Nov 09, 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
    12th Annual Meeting DIA Japan 2015 Nov 15, 2015 Meetings Japan Tokyo, Japan
    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