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    Name Start Date Credits Format Region Location
    Expert Reactor Panel: IOM Report on Sharing Clinical Trial Data May 5, 2015 Online Instruction Global Online
    Novel Data Sources: The Positive Impact of Social Media and Online Networks for Engaging with Patients May 5, 2015 Online Instruction Global Online
    Generic Drug Labeling Proposed Rule and Safety Updates May 5, 2015 Online Instruction Global Online
    FDA’s Evolving Position on the Brief Summary and Adequate Directions for Use Guidance May 5, 2015 Online Instruction Global Online
    Target Product Profile – Strategies to Optimize Drug Development, Product Labeling, and Commercialization May 5, 2015 Online Instruction Global Online
    GVP Module IX Compliant Signal Management Systems in Pharmacovigilance: A Tale of Two Experiences May 5, 2015 Online Instruction Global Online
    Complimentary Webinar - Using Revolutionary Machine Learning to Find the Most Relevant Content to Drive Informed Decisions in Regulatory Intelligence May 5, 2015 Online Instruction Global Online
    Implementation of the FDASIA Patient Provisions May 5, 2015 Online Instruction Global Online
    Complimentary: Regulatory and Real World Evidence Challenges of Rare Diseases and Orphan Drugs May 5, 2015 Online Instruction Global Online
    FDA’s Role in Advancing the Science of Pharmacovigilance: Tools, Methods, and Pilot Programs Under Evaluation for the Analysis of Safety Signals May 5, 2015 Online Instruction Global Online
    Variations in the European Union: CMC/Quality Changes May 5, 2015 Online Instruction Global Online
    Proarrhythmia May 5, 2015 Online Instruction Global Online
    Facets of Drug-Induced Kidney Injury and Regulatory Perspective May 5, 2015 Online Instruction Global Online
    Impact on Drug Development of Novel Translational Safety Biomarkers for Improved Detection of Drug-Induced Acute Kidney Injury May 5, 2015 Online Instruction Global Online
    Pharmacovigilance and Risk Management: Patient Perspective May 5, 2015 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 1: Fundamentals of Clinical Pharmacology: Pharmacokinetics May 5, 2015 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 2: Fundamentals of Clinical Pharmacology: Pharmacodynamics May 5, 2015 Online Instruction Global Online
    Pharmacovigilance and Global Harmonization Updates May 5, 2015 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology For Drug Development - Part 3: Principles of Modeling and Simulation May 5, 2015 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 4: Determining the Safe First Human Dose May 5, 2015 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 5: Assessment of QT Prolongation May 5, 2015 Online Instruction Global Online
    Implementation and Status of Periodic Benefit-Risk Evaluation Reporting (PBRER) in Canada May 5, 2015 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 6: Preclinical Toxicology & Safety May 5, 2015 Online Instruction Global Online
    Complimentary - Need to Reinvent the Clinical Trial? Innovate, Collaborate & Integrate May 5, 2015 Online Instruction Global Online
    Complimentary Webinar - How to Cut Clinical Trial Timelines in Half May 5, 2015 Online Instruction Global Online
    Disruptive Innovation in Medical Information May 5, 2015 Online Instruction Global Online
    Implementing Risk-Based Monitoring: Practical Approaches May 5, 2015 Online Instruction Global Online
    Complimentary - Innovative Strategies for Developing Safer Cancer Therapies May 5, 2015 Online Instruction Global Online
    Complimentary - Risk-Based Monitoring: Regulatory Expectation and Operational Application May 5, 2015 Online Instruction Global Online
    Postmarketing Requirements: The Legal Framework, How They Are Issued, Sponsor Obligations and Challenges to Overcome May 5, 2015 Online Instruction Global Online
    Complementary - How New Electronic Trial Master File (eTMF) Data Standards Can Enhance Clinical Trial Efficiency and Quality May 5, 2015 Online Instruction Global Online
    Complimentary - Regulatory Solutions in the Cloud - 10 Questions You Can't Afford NOT to Ask May 5, 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 May 5, 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 May 5, 2015 Online Instruction Global Online
    Complimentary - From the Clinic to the CFO: Adaptive Trials and Financial Decision-Making May 5, 2015 Online Instruction Global Online
    Complimentary - The Affiliate Challenge – How to Improve Compliance and Efficiency when Working with Regional Affiliates May 5, 2015 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 1: Overall Challenge: The Vision of Better Medicines for Children May 5, 2015 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 3: Regulatory Framework EU May 5, 2015 Online Instruction Global Online
    Seven-Part Pediatric Drug Development Webinar Series - Part 4: Dosing in Children May 5, 2015 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 2: Regulatory Framework US Overview May 5, 2015 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 5: Technical Development: Pediatric Formulations May 5, 2015 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 7: Operational Challenges of Pediatric Clinical Trials May 5, 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 May 5, 2015 Online Instruction Global Online