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    Name Start Date Credits Format Region Location
    Clinical Investigator: Module 2 - Conducting the Study Mar 30, 2015 ACPE, CME Online Instruction North America Online
    Clinical Investigator: Module 1 - Study Preparation and Initiation Mar 30, 2015 ACPE, CME Online Instruction North America Online
    Informed Consent Mar 30, 2015 ACPE Online Instruction North America Online
    Crisis Management Mar 30, 2015 ACPE, IACET Online Instruction North America Online
    Database Management Mar 30, 2015 ACPE, IACET Online Instruction North America Online
    Literature Evaluation Mar 30, 2015 ACPE, IACET Online Instruction North America Online
    Literature Searching Mar 30, 2015 ACPE, IACET Online Instruction North America Online
    Medical Inquiries Mar 30, 2015 ACPE, IACET Online Instruction North America Online
    Medical Writing Mar 30, 2015 IACET Online Instruction North America Online
    Product Labeling Mar 30, 2015 ACPE, IACET Online Instruction North America Online
    Regulatory Issues Mar 30, 2015 ACPE, IACET Online Instruction North America Online
    Statistics for Medical Communications Professionals Mar 30, 2015 ACPE, IACET Online Instruction North America Online
    Drug Safety Regulatory Requirements Mar 30, 2015 ACPE, IACET Online Instruction Global Online
    Premarketing Clinical Trial Safety Mar 30, 2015 ACPE, IACET Online Instruction Global Online
    Postmarketing Safety Management Mar 30, 2015 ACPE, IACET Online Instruction Global Online
    Basics of Signal Detection and Pharmacoepidemiology Mar 30, 2015 ACPE, IACET Online Instruction Global Online
    Safety Audits and Inspections Mar 30, 2015 ACPE, IACET Online Instruction Global Online
    Introduction to Drug Safety Mar 30, 2015 ACPE, IACET Online Instruction Global Online
    A Tour of FDA Mar 30, 2015 Online Instruction Global Online
    A Tour of Health Canada Mar 30, 2015 Online Instruction Global Online
    A Tour of Health Europe Mar 30, 2015 Online Instruction Global Online
    Aspects of Regulatory History Mar 30, 2015 Online Instruction Global Online
    Bioresearch Monitoring Program (BIMO): Introduction Mar 30, 2015 Online Instruction Global Online
    The Clinical Development Process: Investigational Product, Plan, and Data Management Mar 30, 2015 Online Instruction Global Online
    Ethical Review Boards Mar 30, 2015 Online Instruction Global Online
    Ethics as the Foundation to Clinical Research Mar 30, 2015 Online Instruction Global Online
    Awareness of FDA Inspections for Pharmaceutical Manufacturers Mar 30, 2015 Online Instruction Global Online
    Biotechnology: An Overview of Compliance Considerations Mar 30, 2015 Online Instruction Global Online
    Change Control Mar 30, 2015 Online Instruction Global Online
    Clinical Trial Audits and Consequences of Non-Compliance Mar 30, 2015 Online Instruction Global Online
    Computerized Systems Inspections in the Medical Device Industry Mar 30, 2015 Online Instruction Global Online
    European Union Clinical Trials Directive Mar 30, 2015 Online Instruction Global Online
    GMP Principals of SOPs Mar 30, 2015 Online Instruction Global Online
    GMP Updates - Enforcement Changes at the New FDA Mar 30, 2015 Online Instruction Global Online
    GMPs for API Bulk Manufacturers Mar 30, 2015 Online Instruction Global Online
    Good Clinical Practices (GCPs) for New Product Investigations Mar 30, 2015 Online Instruction Global Online
    Good Laboratory Practices (GLPs) Mar 30, 2015 Online Instruction Global Online
    GxPs Mar 30, 2015 Online Instruction Global Online
    HIPAA - The Impact on Clinical Research Mar 30, 2015 Online Instruction Global Online
    Introduction to GMPs Mar 30, 2015 Online Instruction Global Online
    Investigational Product Development Mar 30, 2015 Online Instruction Global Online
    ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials Mar 30, 2015 Online Instruction Global Online
    Key Concepts of Process Validation Mar 30, 2015 Online Instruction Global Online
    Laboratory Specimens for Clinical Research Mar 30, 2015 Online Instruction Global Online
    Medical Device Safety Reporting Mar 30, 2015 Online Instruction Global Online
    Orientation to GMP Compliance Mar 30, 2015 Online Instruction Global Online
    Overview of the Clinical Research Process Mar 30, 2015 Online Instruction Global Online
    Part 11: Electronic Records and Signatures - Application Mar 30, 2015 Online Instruction Global Online
    Part 11: Electronic Records; Electronic Signatures Mar 30, 2015 Online Instruction Global Online
    Principles of Good Documentation Mar 30, 2015 Online Instruction Global Online
    Protection of Human Subjects in Clinical Trials Mar 30, 2015 Online Instruction Global Online
    Selecting and Managing Clinical Contract Research Organizations (CROs) Mar 30, 2015 Online Instruction Global Online
    Understanding Post-Approval Changes Mar 30, 2015 Online Instruction Global Online
    Computerized Systems Inspections in the Pharmaceutical Industry Mar 30, 2015 Online Instruction Global Online
    Basics of the PhRMA Code Mar 30, 2015 Online Instruction Global Online
    Basics of AdvaMed Code Mar 30, 2015 Online Instruction Global Online
    Eucomed Guidelines on Interactions with Healthcare Professionals Mar 30, 2015 Online Instruction Global Online
    Introduction to Medical Device Health Care Compliance Mar 30, 2015 Online Instruction Global Online
    Foreign Corrupt Practices Act Mar 30, 2015 Online Instruction Global Online
    Global Anti-bribery Mar 30, 2015 Online Instruction Global Online
    Variations to Marketing Authorisation in Europe Mar 30, 2015 Online Instruction Global Online
    Registration of Monoclonal Antibodies Mar 30, 2015 Online Instruction Global Online
    How to Gain Approval to Market a Generic Medicinal Product in the USA Mar 30, 2015 Online Instruction Global Online
    Pharmacokinetics and Pharmacodynamics in Drug Registration Mar 30, 2015 Online Instruction Global Online
    Introduction to the European Union Institutions and Regulatory Authority Mar 30, 2015 Online Instruction Global Online
    Introduction to US Institutions and Regulatory Authority (FDA) Mar 30, 2015 Online Instruction Global Online
    Introduction to Japanese Institutions and Regulatory Authorities Mar 30, 2015 Online Instruction Global Online
    Overview of the CTD and eCTD Mar 30, 2015 Online Instruction Global Online
    Introduction to the International Conference on Harmonisation (ICH) Mar 30, 2015 Online Instruction Global Online
    The Regulatory Development of a Drug Mar 30, 2015 Online Instruction Global Online
    Basics of Clinical Trials Mar 30, 2015 Online Instruction Global Online
    How to Register Medicinal Products through the Centralized Procedure Mar 30, 2015 Online Instruction Global Online
    How to Register Medicinal Products through the Mutual Recognition Procedure Mar 30, 2015 Online Instruction Global Online
    How to Maintain Marketing Approvals in Europe for Centrally Authorised Products Mar 30, 2015 Online Instruction Global Online
    How to Register a New Drug in the USA Mar 30, 2015 Online Instruction Global Online
    How to Register Medicinal Products through the Decentralized Procedure Mar 30, 2015 Online Instruction Global Online
    Access to Unapproved Drugs through Compassionate Use Mar 30, 2015 Online Instruction Global Online
    Regulatory Requirements for the Conduct of Clinical Trials in Europe Mar 30, 2015 Online Instruction Global Online
    Orphan Drugs in the USA, European Union, and Japan Mar 30, 2015 Online Instruction Global Online
    Regulatory Requirements for the Submission of Investigational New Drug Applications in the USA (INDs) Mar 30, 2015 Online Instruction Global Online
    Meeting Opportunities with Regulatory Agencies Mar 30, 2015 Online Instruction Global Online