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    Name Start Date Credits Format Region Location
    The Use of Mobile Medical Applications as Companions Sep 30, 2014 Online Instruction Global Online
    Generic Drug Labeling Proposed Rule and Safety Updates Sep 30, 2014 Online Instruction Global Online
    Emerging Technologies to Rare Disorder Drug Development: Promises and Pitfalls Sep 30, 2014 Online Instruction Global Online
    Big Data: Impact of Health Care Reform on Collaborations and Strategies Sep 30, 2014 Online Instruction Global Online
    Implementation of the FDASIA Patient Provisions Sep 30, 2014 Online Instruction Global Online
    Complimentary: Regulatory and Real World Evidence Challenges of Rare Diseases and Orphan Drugs Sep 30, 2014 Online Instruction Global Online
    Variations in the European Union: CMC/Quality Changes Sep 30, 2014 Online Instruction Global Online
    Good Pharmacovigilance Practice: How Good has it Proven to be for Industry? Sep 30, 2014 Online Instruction Global Online
    Pharmacovigilance and Risk Management: Patient Perspective Sep 30, 2014 Online Instruction Global Online
    Complimentary Patient-Centeredness and Engagement in Clinical Research: Opportunities for Industry Sep 30, 2014 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 1: Fundamentals of Clinical Pharmacology: Pharmacokinetics Sep 30, 2014 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 2: Fundamentals of Clinical Pharmacology: Pharmacodynamics Sep 30, 2014 Online Instruction Global Online
    Pharmacovigilance and Global Harmonization Updates Sep 30, 2014 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology For Drug Development - Part 3: Principles of Modeling and Simulation Sep 30, 2014 Online Instruction Global Online
    Designed for Success: Utilizing Protocol Quality by Design (QbD) to Plan Clinical Studies Sep 30, 2014 Online Instruction Global Online
    China Update: Regulatory Changes and Implications Sep 30, 2014 Online Instruction Global Online
    Evaluation and Management of Cardiac Conditions in Oncology Patients Sep 30, 2014 Online Instruction Global Online
    Risk Management of Medicinal Products: REMS and RMP - Need for Harmonization Within the ICH Region? Sep 30, 2014 Online Instruction Global Online
    CardioVascular Safety: The New Paradigm - Proarrhythmic Assessment of New Drugs without the Thorough QT Study Sep 30, 2014 Online Instruction Global Online
    CardioVascular Safety – What are the Key Issues Regarding Blood Pressure Assessment During Clinical Development Sep 30, 2014 Online Instruction Global Online
    Introductory Principles and Application of Risk Management within Clinical Operations Sep 30, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part VI: Preclinical Toxicology & Safety Sep 30, 2014 Online Instruction Global Online
    Electronic Submissions 101 – Essential MS Word and Adobe Acrobat Tools/Skills and Current IT Options Sep 30, 2014 Online Instruction Global Online
    Complimentary - Planning and Implementing Large Cardiovascular Outcomes Studies: Opportunities & Challenges Sep 30, 2014 Online Instruction Global Online
    Complimentary - Press the Easy Button – Ensure Consistency and Compliance for your Documents through Automation Sep 30, 2014 Online Instruction Global Online
    Complimentary - When Outsourcing Stops Making Sense Sep 30, 2014 Online Instruction Global Online
    Complimentary Quintiles/DIA Webinar - Giving Your Study The Right Start Toward Success Through Optimal Country and Site Selection Sep 30, 2014 Online Instruction Global Online
    Complimentary - Risk-Based Monitoring: Regulatory Expectation and Operational Application Sep 30, 2014 Online Instruction Global Online
    Combination Products and Convergence: An Overview of Clinical Benefits, Regulatory Issues & Manufacturing Challenges Sep 30, 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 Sep 30, 2014 Online Instruction Global Online
    Strategies for Successfully Introducing REMS to Your Organization: From Development and Implementation and Internal and External Evaluation Sep 30, 2014 Online Instruction Global Online
    The Case of the New England Compounding Center: Learning from the Tragedy Sep 30, 2014 Online Instruction Global Online
    Complimentary - From the Clinic to the CFO: Adaptive Trials and Financial Decision-Making Sep 30, 2014 Online Instruction Global Online
    Complimentary - The Affiliate Challenge – How to Improve Compliance and Efficiency when Working with Regional Affiliates Sep 30, 2014 Online Instruction Global Online
    The Future of Personalized Medicine and Companion Diagnostics Sep 30, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 1: Overall Challenge: The Vision of Better Medicines for Children Sep 30, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 3: Regulatory Framework EU Sep 30, 2014 Online Instruction Global Online
    Seven-Part Pediatric Drug Development Webinar Series - Part 4: Dosing in Children Sep 30, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 2 Regulatory Framework US Overview Sep 30, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 5: Technical Development: Pediatric Formulations Sep 30, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part VII: Operational Challenges of Pediatric Clinical Trials Sep 30, 2014 Online Instruction Global Online