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    Name Start Date Credits Format Region Location
    The Use of Mobile Medical Applications as Companions Aug 02, 2014 Online Instruction Global Online
    Generic Drug Labeling Proposed Rule and Safety Updates Aug 02, 2014 Online Instruction Global Online
    English Literacy and Spanish Transcreation of Patient Documents: Concepts for Low Literacy Materials Aug 02, 2014 Online Instruction Global Online
    Emerging Technologies to Rare Disorder Drug Development: Promises and Pitfalls Aug 02, 2014 Online Instruction Global Online
    Big Data: Impact of Health Care Reform on Collaborations and Strategies Aug 02, 2014 Online Instruction Global Online
    Implementation of the FDASIA Patient Provisions Aug 02, 2014 Online Instruction Global Online
    Complimentary: Regulatory and Real World Evidence Challenges of Rare Diseases and Orphan Drugs Aug 02, 2014 Online Instruction Global Online
    Variations in the European Union: CMC/Quality Changes Aug 02, 2014 Online Instruction Global Online
    Good Pharmacovigilance Practice: How Good has it Proven to be for Industry? Aug 02, 2014 Online Instruction Global Online
    Safety and Social Media: Is this the Question or the Answer Aug 02, 2014 Online Instruction Global Online
    Pharmacovigilance and Risk Management: Patient Perspective Aug 02, 2014 Online Instruction Global Online
    Complimentary Patient-Centeredness and Engagement in Clinical Research: Opportunities for Industry Aug 02, 2014 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 1: Fundamentals of Clinical Pharmacology: Pharmacokinetics Aug 02, 2014 Online Instruction Global Online
    Pharmacovigilance and Global Harmonization Updates Aug 02, 2014 Online Instruction Global Online
    Designed for Success: Utilizing Protocol Quality by Design (QbD) to Plan Clinical Studies Aug 02, 2014 Online Instruction Global Online
    China Update: Regulatory Changes and Implications Aug 02, 2014 Online Instruction Global Online
    Evaluation and Management of Cardiac Conditions in Oncology Patients Aug 02, 2014 Online Instruction Global Online
    Risk Management of Medicinal Products: REMS and RMP - Need for Harmonization Within the ICH Region? Aug 02, 2014 Online Instruction Global Online
    Complimentary Biomarker Strategies for More Efficient Early-Phase Drug Development in Alzheimer's Disease Aug 02, 2014 Online Instruction Global Online
    CardioVascular Safety: The New Paradigm - Proarrhythmic Assessment of New Drugs without the Thorough QT Study Aug 02, 2014 Online Instruction Global Online
    CardioVascular Safety – What are the Key Issues Regarding Blood Pressure Assessment During Clinical Development Aug 02, 2014 Online Instruction Global Online
    Introductory Principles and Application of Risk Management within Clinical Operations Aug 02, 2014 Online Instruction Global Online
    Electronic Submissions 101 – Essential MS Word and Adobe Acrobat Tools/Skills and Current IT Options Aug 02, 2014 Online Instruction Global Online
    Measurement in Clinical Trials: An Examination of the FDA Position on Review of Clinical Outcome Assessments (COAs) Aug 02, 2014 Online Instruction Global Online
    The Electronic Trial Master File: So Much More than Just a Secure Document Repository Aug 02, 2014 Online Instruction Global Online
    Planning and Implementing Large Cardiovascular Outcomes Studies: Opportunities & Challenges Aug 02, 2014 Online Instruction Global Online
    Press the Easy Button – Ensure Consistency and Compliance for your Documents through Automation Aug 02, 2014 Online Instruction Global Online
    When Outsourcing Stops Making Sense Aug 02, 2014 Online Instruction Global Online
    Complimentary Quintiles/DIA Webinar - Giving Your Study The Right Start Toward Success Through Optimal Country and Site Selection Aug 02, 2014 Online Instruction Global Online
    Complimentary - Risk-Based Monitoring: Regulatory Expectation and Operational Application Aug 02, 2014 Online Instruction Global Online
    A Regulatory Perspective of Biosimilars in Emerging Markets Aug 02, 2014 Online Instruction Global Online
    Combination Products and Convergence: An Overview of Clinical Benefits, Regulatory Issues & Manufacturing Challenges Aug 02, 2014 Online Instruction Global Online
    Strategies for Successfully Introducing REMS to Your Organization: From Development and Implementation and Internal and External Evaluation Aug 02, 2014 Online Instruction Global Online
    The Case of the New England Compounding Center: Learning from the Tragedy Aug 02, 2014 Online Instruction Global Online
    Complimentary - From the Clinic to the CFO: Adaptive Trials and Financial Decision-Making Aug 02, 2014 Online Instruction Global Online
    Complimentary - The Affiliate Challenge – How to Improve Compliance and Efficiency when Working with Regional Affiliates Aug 02, 2014 Online Instruction Global Online
    The Future of Personalized Medicine and Companion Diagnostics Aug 02, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 1: Overall Challenge: The Vision of Better Medicines for Children Aug 02, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 3: Regulatory Framework EU Aug 02, 2014 Online Instruction Global Online
    Seven-Part Pediatric Drug Development Webinar Series - Part 4: Dosing in Children Aug 02, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 2 Regulatory Framework US Overview Aug 02, 2014 Online Instruction Global Online
    The Current State of Quality Oversight (QO) in the Pharmaceutical Industry Aug 02, 2014 Online Instruction Global Online