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