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    Name Start Date Credits Format Region Location
    Clinical Investigator: Module 2 - Conducting the Study Jul 4, 2015 ACPE, CME Online Instruction North America Online
    Clinical Investigator: Module 1 - Study Preparation and Initiation Jul 4, 2015 ACPE, CME Online Instruction North America Online
    Informed Consent Jul 4, 2015 ACPE Online Instruction North America Online
    Crisis Management Jul 4, 2015 ACPE, IACET Online Instruction North America Online
    Database Management Jul 4, 2015 ACPE, IACET Online Instruction North America Online
    Literature Evaluation Jul 4, 2015 ACPE, IACET Online Instruction North America Online
    Literature Searching Jul 4, 2015 ACPE, IACET Online Instruction North America Online
    Medical Inquiries Jul 4, 2015 ACPE, IACET Online Instruction North America Online
    Medical Writing Jul 4, 2015 IACET Online Instruction North America Online
    Product Labeling Jul 4, 2015 ACPE, IACET Online Instruction North America Online
    Regulatory Issues Jul 4, 2015 ACPE, IACET Online Instruction North America Online
    Statistics for Medical Communications Professionals Jul 4, 2015 ACPE, IACET Online Instruction North America Online
    Drug Safety Regulatory Requirements Jul 4, 2015 ACPE, IACET Online Instruction Global Online
    Premarketing Clinical Trial Safety Jul 4, 2015 ACPE, IACET Online Instruction Global Online
    Postmarketing Safety Management Jul 4, 2015 ACPE, IACET Online Instruction Global Online
    Basics of Signal Detection and Pharmacoepidemiology Jul 4, 2015 ACPE, IACET Online Instruction Global Online
    Safety Audits and Inspections Jul 4, 2015 ACPE, IACET Online Instruction Global Online
    Introduction to Drug Safety Jul 4, 2015 ACPE, IACET Online Instruction Global Online
    A Tour of FDA Jul 4, 2015 Online Instruction Global Online
    A Tour of Health Canada Jul 4, 2015 Online Instruction Global Online
    A Tour of Health Europe Jul 4, 2015 Online Instruction Global Online
    Aspects of Regulatory History Jul 4, 2015 Online Instruction Global Online
    Bioresearch Monitoring Program (BIMO): Introduction Jul 4, 2015 Online Instruction Global Online
    The Clinical Development Process: Investigational Product, Plan, and Data Management Jul 4, 2015 Online Instruction Global Online
    Ethical Review Boards Jul 4, 2015 Online Instruction Global Online
    Ethics as the Foundation to Clinical Research Jul 4, 2015 Online Instruction Global Online
    Awareness of FDA Inspections for Pharmaceutical Manufacturers Jul 4, 2015 Online Instruction Global Online
    Biotechnology: An Overview of Compliance Considerations Jul 4, 2015 Online Instruction Global Online
    Change Control Jul 4, 2015 Online Instruction Global Online
    Clinical Trial Audits and Consequences of Non-Compliance Jul 4, 2015 Online Instruction Global Online
    Computerized Systems Inspections in the Medical Device Industry Jul 4, 2015 Online Instruction Global Online
    European Union Clinical Trials Directive Jul 4, 2015 Online Instruction Global Online
    GMP Principals of SOPs Jul 4, 2015 Online Instruction Global Online
    GMP Updates - Enforcement Changes at the New FDA Jul 4, 2015 Online Instruction Global Online
    GMPs for API Bulk Manufacturers Jul 4, 2015 Online Instruction Global Online
    Good Clinical Practices (GCPs) for New Product Investigations Jul 4, 2015 Online Instruction Global Online
    Good Laboratory Practices (GLPs) Jul 4, 2015 Online Instruction Global Online
    GxPs Jul 4, 2015 Online Instruction Global Online
    HIPAA - The Impact on Clinical Research Jul 4, 2015 Online Instruction Global Online
    Introduction to GMPs Jul 4, 2015 Online Instruction Global Online
    Investigational Product Development Jul 4, 2015 Online Instruction Global Online
    ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials Jul 4, 2015 Online Instruction Global Online
    Key Concepts of Process Validation Jul 4, 2015 Online Instruction Global Online
    Laboratory Specimens for Clinical Research Jul 4, 2015 Online Instruction Global Online
    Medical Device Safety Reporting Jul 4, 2015 Online Instruction Global Online
    Orientation to GMP Compliance Jul 4, 2015 Online Instruction Global Online
    Overview of the Clinical Research Process Jul 4, 2015 Online Instruction Global Online
    Part 11: Electronic Records and Signatures - Application Jul 4, 2015 Online Instruction Global Online
    Part 11: Electronic Records; Electronic Signatures Jul 4, 2015 Online Instruction Global Online
    Principles of Good Documentation Jul 4, 2015 Online Instruction Global Online
    Protection of Human Subjects in Clinical Trials Jul 4, 2015 Online Instruction Global Online
    Selecting and Managing Clinical Contract Research Organizations (CROs) Jul 4, 2015 Online Instruction Global Online
    Understanding Post-Approval Changes Jul 4, 2015 Online Instruction Global Online
    Computerized Systems Inspections in the Pharmaceutical Industry Jul 4, 2015 Online Instruction Global Online
    Basics of the PhRMA Code Jul 4, 2015 Online Instruction Global Online
    Basics of AdvaMed Code Jul 4, 2015 Online Instruction Global Online
    Eucomed Guidelines on Interactions with Healthcare Professionals Jul 4, 2015 Online Instruction Global Online
    Introduction to Medical Device Health Care Compliance Jul 4, 2015 Online Instruction Global Online
    Foreign Corrupt Practices Act Jul 4, 2015 Online Instruction Global Online
    Global Anti-bribery Jul 4, 2015 Online Instruction Global Online
    Variations to Marketing Authorisation in Europe Jul 4, 2015 Online Instruction Global Online
    Registration of Monoclonal Antibodies Jul 4, 2015 Online Instruction Global Online
    How to Gain Approval to Market a Generic Medicinal Product in the USA Jul 4, 2015 Online Instruction Global Online
    Pharmacokinetics and Pharmacodynamics in Drug Registration Jul 4, 2015 Online Instruction Global Online
    Overview of Drug Development Jul 4, 2015 IACET, PMI Online Instruction Global Online
    Discovery and Preclinical Testing Phases Jul 4, 2015 Online Instruction Global Online
    Phase 1 Studies Jul 4, 2015 Online Instruction Global Online
    Phase 2 Studies Jul 4, 2015 Online Instruction Global Online
    Phase 3 Studies and Regulatory Review Jul 4, 2015 Online Instruction Global Online
    Phase 4 and Life Cycle Management Jul 4, 2015 Online Instruction Global Online
    Introduction to the European Union Institutions and Regulatory Authority Jul 4, 2015 Online Instruction Global Online
    Introduction to US Institutions and Regulatory Authority (FDA) Jul 4, 2015 Online Instruction Global Online
    Introduction to Japanese Institutions and Regulatory Authorities Jul 4, 2015 Online Instruction Global Online
    Overview of the CTD and eCTD Jul 4, 2015 Online Instruction Global Online
    Introduction to the International Conference on Harmonisation (ICH) Jul 4, 2015 Online Instruction Global Online
    The Regulatory Development of a Drug Jul 4, 2015 Online Instruction Global Online
    Basics of Clinical Trials Jul 4, 2015 Online Instruction Global Online
    How to Register Medicinal Products through the Centralized Procedure Jul 4, 2015 Online Instruction Global Online
    How to Register Medicinal Products through the Mutual Recognition Procedure Jul 4, 2015 Online Instruction Global Online
    How to Maintain Marketing Approvals in Europe for Centrally Authorised Products Jul 4, 2015 Online Instruction Global Online
    How to Register a New Drug in the USA Jul 4, 2015 Online Instruction Global Online
    How to Register Medicinal Products through the Decentralized Procedure Jul 4, 2015 Online Instruction Global Online
    Access to Unapproved Drugs through Compassionate Use Jul 4, 2015 Online Instruction Global Online
    Regulatory Requirements for the Conduct of Clinical Trials in Europe Jul 4, 2015 Online Instruction Global Online
    Orphan Drugs in the USA, European Union, and Japan Jul 4, 2015 Online Instruction Global Online
    Regulatory Requirements for the Submission of Investigational New Drug Applications in the USA (INDs) Jul 4, 2015 Online Instruction Global Online
    Meeting Opportunities with Regulatory Agencies Jul 4, 2015 Online Instruction Global Online