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    Name Start Date Credits Format Region Location
    The Use of Mobile Medical Applications as Companions Oct 21, 2014 Online Instruction Global Online
    Generic Drug Labeling Proposed Rule and Safety Updates Oct 21, 2014 Online Instruction Global Online
    Emerging Technologies to Rare Disorder Drug Development: Promises and Pitfalls Oct 21, 2014 Online Instruction Global Online
    Big Data: Impact of Health Care Reform on Collaborations and Strategies Oct 21, 2014 Online Instruction Global Online
    Implementation of the FDASIA Patient Provisions Oct 21, 2014 Online Instruction Global Online
    Complimentary: Regulatory and Real World Evidence Challenges of Rare Diseases and Orphan Drugs Oct 21, 2014 Online Instruction Global Online
    Variations in the European Union: CMC/Quality Changes Oct 21, 2014 Online Instruction Global Online
    Good Pharmacovigilance Practice: How Good has it Proven to be for Industry? Oct 21, 2014 Online Instruction Global Online
    Pharmacovigilance and Risk Management: Patient Perspective Oct 21, 2014 Online Instruction Global Online
    Complimentary Patient-Centeredness and Engagement in Clinical Research: Opportunities for Industry Oct 21, 2014 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 1: Fundamentals of Clinical Pharmacology: Pharmacokinetics Oct 21, 2014 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 2: Fundamentals of Clinical Pharmacology: Pharmacodynamics Oct 21, 2014 Online Instruction Global Online
    Pharmacovigilance and Global Harmonization Updates Oct 21, 2014 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology For Drug Development - Part 3: Principles of Modeling and Simulation Oct 21, 2014 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 4: Determining the Safe First Human Dose Oct 21, 2014 Online Instruction Global Online
    Designed for Success: Utilizing Protocol Quality by Design (QbD) to Plan Clinical Studies Oct 21, 2014 Online Instruction Global Online
    China Update: Regulatory Changes and Implications Oct 21, 2014 Online Instruction Global Online
    Evaluation and Management of Cardiac Conditions in Oncology Patients Oct 21, 2014 Online Instruction Global Online
    CardioVascular Safety: The New Paradigm - Proarrhythmic Assessment of New Drugs without the Thorough QT Study Oct 21, 2014 Online Instruction Global Online
    CardioVascular Safety – What are the Key Issues Regarding Blood Pressure Assessment During Clinical Development Oct 21, 2014 Online Instruction Global Online
    Introductory Principles and Application of Risk Management within Clinical Operations Oct 21, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 6: Preclinical Toxicology & Safety Oct 21, 2014 Online Instruction Global Online
    Electronic Submissions 101 – Essential MS Word and Adobe Acrobat Tools/Skills and Current IT Options Oct 21, 2014 Online Instruction Global Online
    Disruptive Innovation in Medical Information Oct 21, 2014 Online Instruction Global Online
    Complimentary - Press the Easy Button – Ensure Consistency and Compliance for your Documents through Automation Oct 21, 2014 Online Instruction Global Online
    Complimentary - When Outsourcing Stops Making Sense Oct 21, 2014 Online Instruction Global Online
    Complimentary Quintiles/DIA Webinar - Giving Your Study The Right Start Toward Success Through Optimal Country and Site Selection Oct 21, 2014 Online Instruction Global Online
    Complimentary - Risk-Based Monitoring: Regulatory Expectation and Operational Application Oct 21, 2014 Online Instruction Global Online
    Combination Products and Convergence: An Overview of Clinical Benefits, Regulatory Issues & Manufacturing Challenges Oct 21, 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 Oct 21, 2014 Online Instruction Global Online
    Strategies for Successfully Introducing REMS to Your Organization: From Development and Implementation and Internal and External Evaluation Oct 21, 2014 Online Instruction Global Online
    The Case of the New England Compounding Center: Learning from the Tragedy Oct 21, 2014 Online Instruction Global Online
    Complimentary - From the Clinic to the CFO: Adaptive Trials and Financial Decision-Making Oct 21, 2014 Online Instruction Global Online
    Complimentary - The Affiliate Challenge – How to Improve Compliance and Efficiency when Working with Regional Affiliates Oct 21, 2014 Online Instruction Global Online
    The Future of Personalized Medicine and Companion Diagnostics Oct 21, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 1: Overall Challenge: The Vision of Better Medicines for Children Oct 21, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 3: Regulatory Framework EU Oct 21, 2014 Online Instruction Global Online
    Seven-Part Pediatric Drug Development Webinar Series - Part 4: Dosing in Children Oct 21, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 2: Regulatory Framework US Overview Oct 21, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 5: Technical Development: Pediatric Formulations Oct 21, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 7: Operational Challenges of Pediatric Clinical Trials Oct 21, 2014 Online Instruction Global Online