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    Name Start Date Credits Format Region Location
    The Use of Mobile Medical Applications as Companions Dec 20, 2014 Online Instruction Global Online
    Generic Drug Labeling Proposed Rule and Safety Updates Dec 20, 2014 Online Instruction Global Online
    Emerging Technologies to Rare Disorder Drug Development: Promises and Pitfalls Dec 20, 2014 Online Instruction Global Online
    Target Product Profile – Strategies to Optimize Drug Development, Product Labeling, and Commercialization Dec 20, 2014 Online Instruction Global Online
    Implementation of the FDASIA Patient Provisions Dec 20, 2014 Online Instruction Global Online
    Complimentary: Regulatory and Real World Evidence Challenges of Rare Diseases and Orphan Drugs Dec 20, 2014 Online Instruction Global Online
    Variations in the European Union: CMC/Quality Changes Dec 20, 2014 Online Instruction Global Online
    Proarrhythmia Dec 20, 2014 Online Instruction Global Online
    Facets of Drug-Induced Kidney Injury and Regulatory Perspective Dec 20, 2014 Online Instruction Global Online
    Impact on Drug Development of Novel Translational Safety Biomarkers for Improved Detection of Drug-Induced Acute Kidney Injury Dec 20, 2014 Online Instruction Global Online
    Pharmacovigilance and Risk Management: Patient Perspective Dec 20, 2014 Online Instruction Global Online
    Complimentary Patient-Centeredness and Engagement in Clinical Research: Opportunities for Industry Dec 20, 2014 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 1: Fundamentals of Clinical Pharmacology: Pharmacokinetics Dec 20, 2014 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 2: Fundamentals of Clinical Pharmacology: Pharmacodynamics Dec 20, 2014 Online Instruction Global Online
    Pharmacovigilance and Global Harmonization Updates Dec 20, 2014 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology For Drug Development - Part 3: Principles of Modeling and Simulation Dec 20, 2014 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 4: Determining the Safe First Human Dose Dec 20, 2014 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 5: Assessment of QT Prolongation Dec 20, 2014 Online Instruction Global Online
    Designed for Success: Utilizing Protocol Quality by Design (QbD) to Plan Clinical Studies Dec 20, 2014 Online Instruction Global Online
    Implementation and Status of Periodic Benefit-Risk Evaluation Reporting (PBRER) in Canada Dec 20, 2014 Online Instruction Global Online
    Introductory Principles and Application of Risk Management within Clinical Operations Dec 20, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 6: Preclinical Toxicology & Safety Dec 20, 2014 Online Instruction Global Online
    Complimentary - Need to Reinvent the Clinical Trial? Innovate, Collaborate & Integrate Dec 20, 2014 Online Instruction Global Online
    Disruptive Innovation in Medical Information Dec 20, 2014 Online Instruction Global Online
    Complimentary Quintiles/DIA Webinar - Giving Your Study The Right Start Toward Success Through Optimal Country and Site Selection Dec 20, 2014 Online Instruction Global Online
    Implementing Risk-Based Monitoring: Practical Approaches Dec 20, 2014 Online Instruction Global Online
    Complimentary - Innovative Strategies for Developing Safer Cancer Therapies Dec 20, 2014 Online Instruction Global Online
    Complimentary - Risk-Based Monitoring: Regulatory Expectation and Operational Application Dec 20, 2014 Online Instruction Global Online
    How New Electronic Trial Master File (eTMF) Data Standards Can Enhance Clinical Trial Efficiency and Quality Dec 20, 2014 Online Instruction Global Online
    Complimentary - Regulatory Solutions in the Cloud - 10 Questions You Can't Afford NOT to Ask Dec 20, 2014 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 Dec 20, 2014 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 Dec 20, 2014 Online Instruction Global Online
    Complimentary - From the Clinic to the CFO: Adaptive Trials and Financial Decision-Making Dec 20, 2014 Online Instruction Global Online
    Complimentary - The Affiliate Challenge – How to Improve Compliance and Efficiency when Working with Regional Affiliates Dec 20, 2014 Online Instruction Global Online
    The Future of Personalized Medicine and Companion Diagnostics Dec 20, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 1: Overall Challenge: The Vision of Better Medicines for Children Dec 20, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 3: Regulatory Framework EU Dec 20, 2014 Online Instruction Global Online
    Seven-Part Pediatric Drug Development Webinar Series - Part 4: Dosing in Children Dec 20, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 2: Regulatory Framework US Overview Dec 20, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 5: Technical Development: Pediatric Formulations Dec 20, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 7: Operational Challenges of Pediatric Clinical Trials Dec 20, 2014 Online Instruction Global Online