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    Name Start Date Credits Format Region Location
    Clinical Investigator: Module 2 - Conducting The Study Jul 25, 2014 ACPE, CME Online Instruction North America Online
    Clinical Investigator: Module 1 - Study Preparation and Initiation Jul 25, 2014 ACPE, CME Online Instruction North America Online
    Informed Consent Jul 25, 2014 ACPE Online Instruction North America Online
    Crisis Management Jul 25, 2014 ACPE, IACET Online Instruction North America Online
    Database Management Jul 25, 2014 ACPE, IACET Online Instruction North America Online
    Literature Evaluation Jul 25, 2014 ACPE, IACET Online Instruction North America Online
    Literature Searching Jul 25, 2014 ACPE, IACET Online Instruction North America Online
    Medical Inquiries Jul 25, 2014 ACPE, IACET Online Instruction North America Online
    Medical Writing Jul 25, 2014 IACET Online Instruction North America Online
    Product Labeling Jul 25, 2014 ACPE, IACET Online Instruction North America Online
    Regulatory Issues Jul 25, 2014 ACPE, IACET Online Instruction North America Online
    Statistics for Medical Communications Professionals Jul 25, 2014 ACPE, IACET Online Instruction North America Online
    Drug Safety Regulatory Requirements Jul 25, 2014 ACPE, IACET Online Instruction Global Online
    Premarketing Clinical Trial Safety Jul 25, 2014 ACPE, IACET Online Instruction Global Online
    Postmarketing Safety Management Jul 25, 2014 Online Instruction Global Online
    Basics of Signal Detection and Pharmacoepidemiology Jul 25, 2014 Online Instruction Global Online
    Safety Audits and Inspections Jul 25, 2014 Online Instruction Global Online
    Introduction to Drug Safety Jul 25, 2014 ACPE, IACET Online Instruction Global Online
    A Tour of FDA Jul 25, 2014 Online Instruction Global Online
    A Tour of Health Canada Jul 25, 2014 Online Instruction Global Online
    A Tour of Health Europe Jul 25, 2014 Online Instruction Global Online
    Aspects of Regulatory History Jul 25, 2014 Online Instruction Global Online
    Bioresearch Monitoring Program (BIMO): Introduction Jul 25, 2014 Online Instruction Global Online
    The Clinical Development Process: Investigational Product, Plan, and Data Management Jul 25, 2014 Online Instruction Global Online
    Drug Safety & Adverse Event Reporting Jul 25, 2014 Online Instruction Global Online
    Ethical Review Boards Jul 25, 2014 Online Instruction Global Online
    Ethics as the Foundation to Clinical Research Jul 25, 2014 Online Instruction Global Online
    Awareness of FDA Inspections for Pharmaceutical Manufacturers Jul 25, 2014 Online Instruction Global Online
    Biotechnology: An Overview of Compliance Considerations Jul 25, 2014 Online Instruction Global Online
    Change Control Jul 25, 2014 Online Instruction Global Online
    Clinical Trial Audits and Consequences of Non-Compliance Jul 25, 2014 Online Instruction Global Online
    Computerized Systems Inspections in the Medical Device Industry Jul 25, 2014 Online Instruction Global Online
    European Union Clinical Trials Directive Jul 25, 2014 Online Instruction Global Online
    GMP Principals of SOPs Jul 25, 2014 Online Instruction Global Online
    GMP Updates - Enforcement Changes at the New FDA Jul 25, 2014 Online Instruction Global Online
    GMPs for API Bulk Manufacturers Jul 25, 2014 Online Instruction Global Online
    Good Clinical Practices (GCPs) for New Product Investigations Jul 25, 2014 Online Instruction Global Online
    Good Laboratory Practices (GLPs) Jul 25, 2014 Online Instruction Global Online
    GxPs Jul 25, 2014 Online Instruction Global Online
    HIPAA - The Impact on Clinical Research Jul 25, 2014 Online Instruction Global Online
    Introduction to GMPs Jul 25, 2014 Online Instruction Global Online
    Investigational Product Development Jul 25, 2014 Online Instruction Global Online
    ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials Jul 25, 2014 Online Instruction Global Online
    Key Concepts of Process Validation Jul 25, 2014 Online Instruction Global Online
    Laboratory Specimens for Clinical Research Jul 25, 2014 Online Instruction Global Online
    Medical Device Safety Reporting Jul 25, 2014 Online Instruction Global Online
    Orientation to GMP Compliance Jul 25, 2014 Online Instruction Global Online
    Overview of the Clinical Research Process Jul 25, 2014 Online Instruction Global Online
    Part 11: Electronic Records and Signatures - Application Jul 25, 2014 Online Instruction Global Online
    Part 11: Electronic Records; Electronic Signatures Jul 25, 2014 Online Instruction Global Online
    Principles of Good Documentation Jul 25, 2014 Online Instruction Global Online
    Protection of Human Subjects in Clinical Trials Jul 25, 2014 Online Instruction Global Online
    Selecting and Managing Clinical Contract Research Organizations (CROs) Jul 25, 2014 Online Instruction Global Online
    Understanding Post-Approval Changes Jul 25, 2014 Online Instruction Global Online
    Computerized Systems Inspections in the Pharmaceutical Industry Jul 25, 2014 Online Instruction Global Online
    Basics of the PhRMA Code Jul 25, 2014 Online Instruction Global Online
    Basics of AdvaMed Code Jul 25, 2014 Online Instruction Global Online
    Eucomed Guidelines on Interactions with Healthcare Professionals Jul 25, 2014 Online Instruction Global Online
    Introduction to Medical Device Health Care Compliance Jul 25, 2014 Online Instruction Global Online
    Foreign Corrupt Practices Act Jul 25, 2014 Online Instruction Global Online
    Global Anti-bribery Jul 25, 2014 Online Instruction Global Online
    Variations to Marketing Authorisation in Europe Jul 25, 2014 Online Instruction Global Online
    Registration of Monoclonal Antibodies Jul 25, 2014 Online Instruction Global Online
    How to Gain Approval to Market a Generic Medicinal Product in the USA Jul 25, 2014 Online Instruction Global Online
    Pharmacokinetics and Pharmacodynamics in Drug Registration Jul 25, 2014 Online Instruction Global Online
    Introduction to the European Union Institutions and Regulatory Authority Jul 25, 2014 Online Instruction Global Online
    Introduction to US Institutions and Regulatory Authority (FDA) Jul 25, 2014 Online Instruction Global Online
    Introduction to Japanese Institutions and Regulatory Authorities Jul 25, 2014 Online Instruction Global Online
    Overview of the CTD and eCTD Jul 25, 2014 Online Instruction Global Online
    Introduction to the International Conference on Harmonisation (ICH) Jul 25, 2014 Online Instruction Global Online
    The Regulatory Development of a Drug Jul 25, 2014 Online Instruction Global Online
    Basics of Clinical Trials Jul 25, 2014 Online Instruction Global Online
    How to Register Medicinal Products through the Centralized Procedure Jul 25, 2014 Online Instruction Global Online
    How to Register Medicinal Products through the Mutual Recognition Procedure Jul 25, 2014 Online Instruction Global Online
    How to Maintain Marketing Approvals in Europe for Centrally Authorised Products Jul 25, 2014 Online Instruction Global Online
    How to Register a New Drug in the USA Jul 25, 2014 Online Instruction Global Online
    How to Register Medicinal Products through the Decentralized Procedure Jul 25, 2014 Online Instruction Global Online
    Access to Unapproved Drugs through Compassionate Use Jul 25, 2014 Online Instruction Global Online
    Regulatory Requirements for the Conduct of Clinical Trials in Europe Jul 25, 2014 Online Instruction Global Online
    Orphan Drugs in the USA, European Union, and Japan Jul 25, 2014 Online Instruction Global Online
    Regulatory Requirements for the Submission of Investigational New Drug Applications in the USA (INDs) Jul 25, 2014 Online Instruction Global Online
    Meeting Opportunities with Regulatory Agencies Jul 25, 2014 Online Instruction Global Online