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    Name Start Date Credits Format Region Location
    The Use of Mobile Medical Applications as Companions Dec 23, 2014 Online Instruction Global Online
    Generic Drug Labeling Proposed Rule and Safety Updates Dec 23, 2014 Online Instruction Global Online
    Emerging Technologies to Rare Disorder Drug Development: Promises and Pitfalls Dec 23, 2014 Online Instruction Global Online
    Target Product Profile – Strategies to Optimize Drug Development, Product Labeling, and Commercialization Dec 23, 2014 Online Instruction Global Online
    The Role of the Clinical Data Manager Dec 23, 2014 Online Instruction Global Online
    Implementation of the FDASIA Patient Provisions Dec 23, 2014 Online Instruction Global Online
    Complimentary: Regulatory and Real World Evidence Challenges of Rare Diseases and Orphan Drugs Dec 23, 2014 Online Instruction Global Online
    Variations in the European Union: CMC/Quality Changes Dec 23, 2014 Online Instruction Global Online
    Proarrhythmia Dec 23, 2014 Online Instruction Global Online
    Facets of Drug-Induced Kidney Injury and Regulatory Perspective Dec 23, 2014 Online Instruction Global Online
    Impact on Drug Development of Novel Translational Safety Biomarkers for Improved Detection of Drug-Induced Acute Kidney Injury Dec 23, 2014 Online Instruction Global Online
    Pharmacovigilance and Risk Management: Patient Perspective Dec 23, 2014 Online Instruction Global Online
    Complimentary Patient-Centeredness and Engagement in Clinical Research: Opportunities for Industry Dec 23, 2014 Online Instruction Global Online
    Drug Safety Regulatory Requirements Dec 23, 2014 ACPE, IACET Online Instruction Global Online
    Premarketing Clinical Trial Safety Dec 23, 2014 ACPE, IACET Online Instruction Global Online
    Postmarketing Safety Management Dec 23, 2014 ACPE, IACET Online Instruction Global Online
    Basics of Signal Detection and Pharmacoepidemiology Dec 23, 2014 ACPE, IACET Online Instruction Global Online
    Safety Audits and Inspections Dec 23, 2014 ACPE, IACET Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 1: Fundamentals of Clinical Pharmacology: Pharmacokinetics Dec 23, 2014 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 2: Fundamentals of Clinical Pharmacology: Pharmacodynamics Dec 23, 2014 Online Instruction Global Online
    Pharmacovigilance and Global Harmonization Updates Dec 23, 2014 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology For Drug Development - Part 3: Principles of Modeling and Simulation Dec 23, 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 23, 2014 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 5: Assessment of QT Prolongation Dec 23, 2014 Online Instruction Global Online
    Designed for Success: Utilizing Protocol Quality by Design (QbD) to Plan Clinical Studies Dec 23, 2014 Online Instruction Global Online
    Negotiation and Influence Dec 23, 2014 Online Instruction Global Online
    Introduction to Drug Safety Dec 23, 2014 ACPE, IACET Online Instruction Global Online
    How to Prepare for a Safety Inspection Dec 23, 2014 Online Instruction Global Online
    Implementation and Status of Periodic Benefit-Risk Evaluation Reporting (PBRER) in Canada Dec 23, 2014 Online Instruction Global Online
    Clinical Statistics for Nonstatisticians Dec 23, 2014 Online Instruction Global Online
    Advanced Clinical Statistics for Nonstatisticians Dec 23, 2014 Online Instruction Global Online
    Development of a Clinical Study Report Dec 23, 2014 Online Instruction Global Online
    Art of Writing a Clinical Overview Dec 23, 2014 Online Instruction Global Online
    Introductory Principles and Application of Risk Management within Clinical Operations Dec 23, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 6: Preclinical Toxicology & Safety Dec 23, 2014 Online Instruction Global Online
    Complimentary - Need to Reinvent the Clinical Trial? Innovate, Collaborate & Integrate Dec 23, 2014 Online Instruction Global Online
    Disruptive Innovation in Medical Information Dec 23, 2014 Online Instruction Global Online
    A Tour of FDA Dec 23, 2014 Online Instruction Global Online
    A Tour of Health Canada Dec 23, 2014 Online Instruction Global Online
    A Tour of Health Europe Dec 23, 2014 Online Instruction Global Online
    Aspects of Regulatory History Dec 23, 2014 Online Instruction Global Online
    Bioresearch Monitoring Program (BIMO): Introduction Dec 23, 2014 Online Instruction Global Online
    The Clinical Development Process: Investigational Product, Plan, and Data Management Dec 23, 2014 Online Instruction Global Online
    Drug Safety & Adverse Event Reporting Dec 23, 2014 Online Instruction Global Online
    Ethical Review Boards Dec 23, 2014 Online Instruction Global Online
    Ethics as the Foundation to Clinical Research Dec 23, 2014 Online Instruction Global Online
    Awareness of FDA Inspections for Pharmaceutical Manufacturers Dec 23, 2014 Online Instruction Global Online
    Biotechnology: An Overview of Compliance Considerations Dec 23, 2014 Online Instruction Global Online
    Change Control Dec 23, 2014 Online Instruction Global Online
    Clinical Trial Audits and Consequences of Non-Compliance Dec 23, 2014 Online Instruction Global Online
    Computerized Systems Inspections in the Medical Device Industry Dec 23, 2014 Online Instruction Global Online
    European Union Clinical Trials Directive Dec 23, 2014 Online Instruction Global Online
    GMP Principals of SOPs Dec 23, 2014 Online Instruction Global Online
    GMP Updates - Enforcement Changes at the New FDA Dec 23, 2014 Online Instruction Global Online
    GMPs for API Bulk Manufacturers Dec 23, 2014 Online Instruction Global Online
    Good Clinical Practices (GCPs) for New Product Investigations Dec 23, 2014 Online Instruction Global Online
    Good Laboratory Practices (GLPs) Dec 23, 2014 Online Instruction Global Online
    GxPs Dec 23, 2014 Online Instruction Global Online
    HIPAA - The Impact on Clinical Research Dec 23, 2014 Online Instruction Global Online
    Introduction to GMPs Dec 23, 2014 Online Instruction Global Online
    Investigational Product Development Dec 23, 2014 Online Instruction Global Online
    ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials Dec 23, 2014 Online Instruction Global Online
    Key Concepts of Process Validation Dec 23, 2014 Online Instruction Global Online
    Laboratory Specimens for Clinical Research Dec 23, 2014 Online Instruction Global Online
    Medical Device Safety Reporting Dec 23, 2014 Online Instruction Global Online
    Orientation to GMP Compliance Dec 23, 2014 Online Instruction Global Online
    Overview of the Clinical Research Process Dec 23, 2014 Online Instruction Global Online
    Part 11: Electronic Records and Signatures - Application Dec 23, 2014 Online Instruction Global Online
    Part 11: Electronic Records; Electronic Signatures Dec 23, 2014 Online Instruction Global Online
    Principles of Good Documentation Dec 23, 2014 Online Instruction Global Online
    Protection of Human Subjects in Clinical Trials Dec 23, 2014 Online Instruction Global Online
    Selecting and Managing Clinical Contract Research Organizations (CROs) Dec 23, 2014 Online Instruction Global Online
    Understanding Post-Approval Changes Dec 23, 2014 Online Instruction Global Online
    Computerized Systems Inspections in the Pharmaceutical Industry Dec 23, 2014 Online Instruction Global Online
    Basics of the PhRMA Code Dec 23, 2014 Online Instruction Global Online
    Basics of AdvaMed Code Dec 23, 2014 Online Instruction Global Online
    Eucomed Guidelines on Interactions with Healthcare Professionals Dec 23, 2014 Online Instruction Global Online
    Introduction to Medical Device Health Care Compliance Dec 23, 2014 Online Instruction Global Online
    Foreign Corrupt Practices Act Dec 23, 2014 Online Instruction Global Online
    Global Anti-bribery Dec 23, 2014 Online Instruction Global Online
    Variations to Marketing Authorisation in Europe Dec 23, 2014 Online Instruction Global Online
    Registration of Monoclonal Antibodies Dec 23, 2014 Online Instruction Global Online
    How to Gain Approval to Market a Generic Medicinal Product in the USA Dec 23, 2014 Online Instruction Global Online
    Pharmacokinetics and Pharmacodynamics in Drug Registration Dec 23, 2014 Online Instruction Global Online
    Complimentary Quintiles/DIA Webinar - Giving Your Study The Right Start Toward Success Through Optimal Country and Site Selection Dec 23, 2014 Online Instruction Global Online
    Implementing Risk-Based Monitoring: Practical Approaches Dec 23, 2014 Online Instruction Global Online
    Complimentary - Innovative Strategies for Developing Safer Cancer Therapies Dec 23, 2014 Online Instruction Global Online
    Complimentary - Risk-Based Monitoring: Regulatory Expectation and Operational Application Dec 23, 2014 Online Instruction Global Online
    Fundamentals of Project Management for Nonproject Managers Dec 23, 2014 Online Instruction Global Online
    Planning and Managing Your Projects Dec 23, 2014 Online Instruction Global Online
    Preparing a Clinical Trial Budget Dec 23, 2014 Online Instruction Global Online
    Team Building and Development Dec 23, 2014 Online Instruction Global Online
    Introduction to the European Union Institutions and Regulatory Authority Dec 23, 2014 Online Instruction Global Online
    Introduction to US Institutions and Regulatory Authority (FDA) Dec 23, 2014 Online Instruction Global Online
    Introduction to Japanese Institutions and Regulatory Authorities Dec 23, 2014 Online Instruction Global Online
    Overview of the CTD and eCTD Dec 23, 2014 Online Instruction Global Online
    Introduction to the International Conference on Harmonisation (ICH) Dec 23, 2014 Online Instruction Global Online
    The Regulatory Development of a Drug Dec 23, 2014 Online Instruction Global Online
    Basics of Clinical Trials Dec 23, 2014 Online Instruction Global Online
    How to Register Medicinal Products through the Centralized Procedure Dec 23, 2014 Online Instruction Global Online
    How to Register Medicinal Products through the Mutual Recognition Procedure Dec 23, 2014 Online Instruction Global Online
    How to Maintain Marketing Approvals in Europe for Centrally Authorised Products Dec 23, 2014 Online Instruction Global Online
    How to Register a New Drug in the USA Dec 23, 2014 Online Instruction Global Online
    How to Register Medicinal Products through the Decentralized Procedure Dec 23, 2014 Online Instruction Global Online
    Access to Unapproved Drugs through Compassionate Use Dec 23, 2014 Online Instruction Global Online
    Regulatory Requirements for the Conduct of Clinical Trials in Europe Dec 23, 2014 Online Instruction Global Online
    Orphan Drugs in the USA, European Union, and Japan Dec 23, 2014 Online Instruction Global Online
    Regulatory Requirements for the Submission of Investigational New Drug Applications in the USA (INDs) Dec 23, 2014 Online Instruction Global Online
    Meeting Opportunities with Regulatory Agencies Dec 23, 2014 Online Instruction Global Online
    How New Electronic Trial Master File (eTMF) Data Standards Can Enhance Clinical Trial Efficiency and Quality Dec 23, 2014 Online Instruction Global Online
    Complimentary - Regulatory Solutions in the Cloud - 10 Questions You Can't Afford NOT to Ask Dec 23, 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 23, 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 23, 2014 Online Instruction Global Online
    Complimentary - From the Clinic to the CFO: Adaptive Trials and Financial Decision-Making Dec 23, 2014 Online Instruction Global Online
    Adverse Event Reporting Requirements: IND and Postmarketing Dec 23, 2014 Online Instruction Global Online
    Complimentary - The Affiliate Challenge – How to Improve Compliance and Efficiency when Working with Regional Affiliates Dec 23, 2014 Online Instruction Global Online
    The Future of Personalized Medicine and Companion Diagnostics Dec 23, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 1: Overall Challenge: The Vision of Better Medicines for Children Dec 23, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 3: Regulatory Framework EU Dec 23, 2014 Online Instruction Global Online
    Seven-Part Pediatric Drug Development Webinar Series - Part 4: Dosing in Children Dec 23, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 2: Regulatory Framework US Overview Dec 23, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 5: Technical Development: Pediatric Formulations Dec 23, 2014 Online Instruction Global Online
    Basics of the IND Dec 23, 2014 Online Instruction Global Online
    Basics of the NDA Dec 23, 2014 Online Instruction Global Online
    Regulatory Aspects of Prescription Drug/Biologics Advertising and Promotional Labeling Dec 23, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 7: Operational Challenges of Pediatric Clinical Trials Dec 23, 2014 Online Instruction Global Online
    Supplements and Other Changes to an Approved Application Dec 23, 2014 Online Instruction Global Online
    Regulatory Aspects of Prescription Drug/Biologics Advertising and Promotional Labeling Feb 05, 2015 IACET Online Instruction Global Online
    Art of Writing a Clinical Overview Feb 24, 2015 IACET Online Instruction Global Online
    Preparing a Clinical Trial Budget Mar 10, 2015 Online Instruction Global Online
    Basics of the IND Phase May 04, 2015 Online Instruction Global Online
    Oversight of Clinical Monitoring: Trends and Strategies May 05, 2015 Online Instruction Global Online
    Basics of the NDA Phase May 18, 2015 Online Instruction Global Online
    How to Prepare for a Safety Inspection Jun 01, 2015 IACET Online Instruction Global Online
    Adverse Event Reporting Requirements: IND and Post-marketing Jul 13, 2015 Online Instruction Global Online
    Interactions with the FDA during IND/NDA Phases Jul 16, 2015 Online Instruction Global Online
    Overview of Drug Development in Japan Sep 02, 2015 Online Instruction Global Online
    Introduction to Signal Detection and Data Mining Oct 05, 2015 Online Instruction Global Online