DIA
Drug Information Association Logo

Advanced Search

MM-DD-YYYY

Add Filter

    Advanced Search

    Find Meetings & Training 

    Name Start Date Credits Format Region Location
    Expert Reactor Panel: IOM Report on Sharing Clinical Trial Data Mar 30, 2015 Online Instruction Global Online
    Novel Data Sources: The Positive Impact of Social Media and Online Networks for Engaging with Patients Mar 30, 2015 Online Instruction Global Online
    Generic Drug Labeling Proposed Rule and Safety Updates Mar 30, 2015 Online Instruction Global Online
    FDA’s Evolving Position on the Brief Summary Mar 30, 2015 Online Instruction Global Online
    Target Product Profile – Strategies to Optimize Drug Development, Product Labeling, and Commercialization Mar 30, 2015 Online Instruction Global Online
    GVP Module IX Compliant Signal Management Systems in Pharmacovigilance: A Tale of Two Experiences Mar 30, 2015 Online Instruction Global Online
    The Role of the Clinical Data Manager Mar 30, 2015 Online Instruction Global Online
    Implementation of the FDASIA Patient Provisions Mar 30, 2015 Online Instruction Global Online
    Complimentary: Regulatory and Real World Evidence Challenges of Rare Diseases and Orphan Drugs Mar 30, 2015 Online Instruction Global Online
    Variations in the European Union: CMC/Quality Changes Mar 30, 2015 Online Instruction Global Online
    Proarrhythmia Mar 30, 2015 Online Instruction Global Online
    Facets of Drug-Induced Kidney Injury and Regulatory Perspective Mar 30, 2015 Online Instruction Global Online
    Impact on Drug Development of Novel Translational Safety Biomarkers for Improved Detection of Drug-Induced Acute Kidney Injury Mar 30, 2015 Online Instruction Global Online
    Pharmacovigilance and Risk Management: Patient Perspective Mar 30, 2015 Online Instruction Global Online
    Drug Safety Regulatory Requirements Mar 30, 2015 ACPE, IACET Online Instruction Global Online
    Premarketing Clinical Trial Safety Mar 30, 2015 ACPE, IACET Online Instruction Global Online
    Postmarketing Safety Management Mar 30, 2015 ACPE, IACET Online Instruction Global Online
    Basics of Signal Detection and Pharmacoepidemiology Mar 30, 2015 ACPE, IACET Online Instruction Global Online
    Safety Audits and Inspections Mar 30, 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 30, 2015 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 2: Fundamentals of Clinical Pharmacology: Pharmacodynamics Mar 30, 2015 Online Instruction Global Online
    Pharmacovigilance and Global Harmonization Updates Mar 30, 2015 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology For Drug Development - Part 3: Principles of Modeling and Simulation Mar 30, 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 30, 2015 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 5: Assessment of QT Prolongation Mar 30, 2015 Online Instruction Global Online
    Designed for Success: Utilizing Protocol Quality by Design (QbD) to Plan Clinical Studies Mar 30, 2015 Online Instruction Global Online
    Negotiation and Influence Mar 30, 2015 Online Instruction Global Online
    Introduction to Drug Safety Mar 30, 2015 ACPE, IACET Online Instruction Global Online
    How to Prepare for a Safety Inspection Mar 30, 2015 Online Instruction Global Online
    Implementation and Status of Periodic Benefit-Risk Evaluation Reporting (PBRER) in Canada Mar 30, 2015 Online Instruction Global Online
    Clinical Statistics for Nonstatisticians Mar 30, 2015 Online Instruction Global Online
    Advanced Clinical Statistics for Nonstatisticians Mar 30, 2015 Online Instruction Global Online
    Development of a Clinical Study Report Mar 30, 2015 Online Instruction Global Online
    Art of Writing a Clinical Overview Mar 30, 2015 Online Instruction Global Online
    Introductory Principles and Application of Risk Management within Clinical Operations Mar 30, 2015 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 6: Preclinical Toxicology & Safety Mar 30, 2015 Online Instruction Global Online
    Complimentary - Need to Reinvent the Clinical Trial? Innovate, Collaborate & Integrate Mar 30, 2015 Online Instruction Global Online
    Complimentary Webinar - How to Cut Clinical Trial Timelines in Half Mar 30, 2015 Online Instruction Global Online
    Disruptive Innovation in Medical Information Mar 30, 2015 Online Instruction Global Online
    A Tour of FDA Mar 30, 2015 Online Instruction Global Online
    A Tour of Health Canada Mar 30, 2015 Online Instruction Global Online
    A Tour of Health Europe Mar 30, 2015 Online Instruction Global Online
    Aspects of Regulatory History Mar 30, 2015 Online Instruction Global Online
    Bioresearch Monitoring Program (BIMO): Introduction Mar 30, 2015 Online Instruction Global Online
    The Clinical Development Process: Investigational Product, Plan, and Data Management Mar 30, 2015 Online Instruction Global Online
    Ethical Review Boards Mar 30, 2015 Online Instruction Global Online
    Ethics as the Foundation to Clinical Research Mar 30, 2015 Online Instruction Global Online
    Awareness of FDA Inspections for Pharmaceutical Manufacturers Mar 30, 2015 Online Instruction Global Online
    Biotechnology: An Overview of Compliance Considerations Mar 30, 2015 Online Instruction Global Online
    Change Control Mar 30, 2015 Online Instruction Global Online
    Clinical Trial Audits and Consequences of Non-Compliance Mar 30, 2015 Online Instruction Global Online
    Computerized Systems Inspections in the Medical Device Industry Mar 30, 2015 Online Instruction Global Online
    European Union Clinical Trials Directive Mar 30, 2015 Online Instruction Global Online
    GMP Principals of SOPs Mar 30, 2015 Online Instruction Global Online
    GMP Updates - Enforcement Changes at the New FDA Mar 30, 2015 Online Instruction Global Online
    GMPs for API Bulk Manufacturers Mar 30, 2015 Online Instruction Global Online
    Good Clinical Practices (GCPs) for New Product Investigations Mar 30, 2015 Online Instruction Global Online
    Good Laboratory Practices (GLPs) Mar 30, 2015 Online Instruction Global Online
    GxPs Mar 30, 2015 Online Instruction Global Online
    HIPAA - The Impact on Clinical Research Mar 30, 2015 Online Instruction Global Online
    Introduction to GMPs Mar 30, 2015 Online Instruction Global Online
    Investigational Product Development Mar 30, 2015 Online Instruction Global Online
    ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials Mar 30, 2015 Online Instruction Global Online
    Key Concepts of Process Validation Mar 30, 2015 Online Instruction Global Online
    Laboratory Specimens for Clinical Research Mar 30, 2015 Online Instruction Global Online
    Medical Device Safety Reporting Mar 30, 2015 Online Instruction Global Online
    Orientation to GMP Compliance Mar 30, 2015 Online Instruction Global Online
    Overview of the Clinical Research Process Mar 30, 2015 Online Instruction Global Online
    Part 11: Electronic Records and Signatures - Application Mar 30, 2015 Online Instruction Global Online
    Part 11: Electronic Records; Electronic Signatures Mar 30, 2015 Online Instruction Global Online
    Principles of Good Documentation Mar 30, 2015 Online Instruction Global Online
    Protection of Human Subjects in Clinical Trials Mar 30, 2015 Online Instruction Global Online
    Selecting and Managing Clinical Contract Research Organizations (CROs) Mar 30, 2015 Online Instruction Global Online
    Understanding Post-Approval Changes Mar 30, 2015 Online Instruction Global Online
    Computerized Systems Inspections in the Pharmaceutical Industry Mar 30, 2015 Online Instruction Global Online
    Basics of the PhRMA Code Mar 30, 2015 Online Instruction Global Online
    Basics of AdvaMed Code Mar 30, 2015 Online Instruction Global Online
    Eucomed Guidelines on Interactions with Healthcare Professionals Mar 30, 2015 Online Instruction Global Online
    Introduction to Medical Device Health Care Compliance Mar 30, 2015 Online Instruction Global Online
    Foreign Corrupt Practices Act Mar 30, 2015 Online Instruction Global Online
    Global Anti-bribery Mar 30, 2015 Online Instruction Global Online
    Variations to Marketing Authorisation in Europe Mar 30, 2015 Online Instruction Global Online
    Registration of Monoclonal Antibodies Mar 30, 2015 Online Instruction Global Online
    How to Gain Approval to Market a Generic Medicinal Product in the USA Mar 30, 2015 Online Instruction Global Online
    Pharmacokinetics and Pharmacodynamics in Drug Registration Mar 30, 2015 Online Instruction Global Online
    Complimentary Quintiles/DIA Webinar - Giving Your Study The Right Start Toward Success Through Optimal Country and Site Selection Mar 30, 2015 Online Instruction Global Online
    Implementing Risk-Based Monitoring: Practical Approaches Mar 30, 2015 Online Instruction Global Online
    Complimentary - Innovative Strategies for Developing Safer Cancer Therapies Mar 30, 2015 Online Instruction Global Online
    Complimentary - Risk-Based Monitoring: Regulatory Expectation and Operational Application Mar 30, 2015 Online Instruction Global Online
    Fundamentals of Project Management for Nonproject Managers Mar 30, 2015 Online Instruction Global Online
    Planning and Managing Your Projects Mar 30, 2015 Online Instruction Global Online
    Team Building and Development Mar 30, 2015 Online Instruction Global Online
    Preparing a Clinical Trial Budget Mar 30, 2015 Online Instruction Global Online
    Introduction to the European Union Institutions and Regulatory Authority Mar 30, 2015 Online Instruction Global Online
    Introduction to US Institutions and Regulatory Authority (FDA) Mar 30, 2015 Online Instruction Global Online
    Introduction to Japanese Institutions and Regulatory Authorities Mar 30, 2015 Online Instruction Global Online
    Overview of the CTD and eCTD Mar 30, 2015 Online Instruction Global Online
    Introduction to the International Conference on Harmonisation (ICH) Mar 30, 2015 Online Instruction Global Online
    The Regulatory Development of a Drug Mar 30, 2015 Online Instruction Global Online
    Basics of Clinical Trials Mar 30, 2015 Online Instruction Global Online
    How to Register Medicinal Products through the Centralized Procedure Mar 30, 2015 Online Instruction Global Online
    How to Register Medicinal Products through the Mutual Recognition Procedure Mar 30, 2015 Online Instruction Global Online
    How to Maintain Marketing Approvals in Europe for Centrally Authorised Products Mar 30, 2015 Online Instruction Global Online
    How to Register a New Drug in the USA Mar 30, 2015 Online Instruction Global Online
    How to Register Medicinal Products through the Decentralized Procedure Mar 30, 2015 Online Instruction Global Online
    Access to Unapproved Drugs through Compassionate Use Mar 30, 2015 Online Instruction Global Online
    Regulatory Requirements for the Conduct of Clinical Trials in Europe Mar 30, 2015 Online Instruction Global Online
    Orphan Drugs in the USA, European Union, and Japan Mar 30, 2015 Online Instruction Global Online
    Regulatory Requirements for the Submission of Investigational New Drug Applications in the USA (INDs) Mar 30, 2015 Online Instruction Global Online
    Meeting Opportunities with Regulatory Agencies Mar 30, 2015 Online Instruction Global Online
    Complementary - How New Electronic Trial Master File (eTMF) Data Standards Can Enhance Clinical Trial Efficiency and Quality Mar 30, 2015 Online Instruction Global Online
    Complimentary - Regulatory Solutions in the Cloud - 10 Questions You Can't Afford NOT to Ask Mar 30, 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 30, 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 30, 2015 Online Instruction Global Online
    Complimentary - From the Clinic to the CFO: Adaptive Trials and Financial Decision-Making Mar 30, 2015 Online Instruction Global Online
    Adverse Event Reporting Requirements: IND and Postmarketing Mar 30, 2015 Online Instruction Global Online
    Complimentary - The Affiliate Challenge – How to Improve Compliance and Efficiency when Working with Regional Affiliates Mar 30, 2015 Online Instruction Global Online
    The Future of Personalized Medicine and Companion Diagnostics Mar 30, 2015 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 1: Overall Challenge: The Vision of Better Medicines for Children Mar 30, 2015 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 3: Regulatory Framework EU Mar 30, 2015 Online Instruction Global Online
    Seven-Part Pediatric Drug Development Webinar Series - Part 4: Dosing in Children Mar 30, 2015 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 2: Regulatory Framework US Overview Mar 30, 2015 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 5: Technical Development: Pediatric Formulations Mar 30, 2015 Online Instruction Global Online
    Basics of the IND Mar 30, 2015 Online Instruction Global Online
    Basics of the NDA Mar 30, 2015 Online Instruction Global Online
    Regulatory Aspects of Prescription Drug/Biologics Advertising and Promotional Labeling Mar 30, 2015 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 7: Operational Challenges of Pediatric Clinical Trials Mar 30, 2015 Online Instruction Global Online
    Supplements and Other Changes to an Approved Application Mar 30, 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 30, 2015 Online Instruction Global Online
    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 - Using Revolutionary Machine Learning to Find the Most Relevant Content to Drive Informed Decisions in Regulatory Intelligence Apr 08, 2015 Online Instruction Global Online
    FDA’s Evolving Position on the Brief Summary Apr 28, 2015 IACET Online Instruction Global Online
    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
    eRegulatory and Intelligence Virtual Conference May 11, 2015 Meetings Global
    Basics of the NDA Phase May 18, 2015 IACET Online Instruction Global Online
    How to Prepare for a Safety Inspection Jun 01, 2015 IACET Online Instruction Global Online
    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
    Overview of Drug Development in Japan Sep 02, 2015 Online Instruction Global Online
    Introduction to Signal Detection and Data Mining Oct 05, 2015 IACET Online Instruction Global Online