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    Name Start Date Credits Format Region Location
    Clinical Investigator: Module 2 - Conducting The Study Jul 26, 2014 ACPE, CME Online Instruction North America Online
    Clinical Investigator: Module 1 - Study Preparation and Initiation Jul 26, 2014 ACPE, CME Online Instruction North America Online
    Informed Consent Jul 26, 2014 ACPE Online Instruction North America Online
    Crisis Management Jul 26, 2014 ACPE, IACET Online Instruction North America Online
    Database Management Jul 26, 2014 ACPE, IACET Online Instruction North America Online
    Literature Evaluation Jul 26, 2014 ACPE, IACET Online Instruction North America Online
    Literature Searching Jul 26, 2014 ACPE, IACET Online Instruction North America Online
    Medical Inquiries Jul 26, 2014 ACPE, IACET Online Instruction North America Online
    Medical Writing Jul 26, 2014 IACET Online Instruction North America Online
    Product Labeling Jul 26, 2014 ACPE, IACET Online Instruction North America Online
    Regulatory Issues Jul 26, 2014 ACPE, IACET Online Instruction North America Online
    Statistics for Medical Communications Professionals Jul 26, 2014 ACPE, IACET Online Instruction North America Online
    Drug Safety Regulatory Requirements Jul 26, 2014 ACPE, IACET Online Instruction Global Online
    Premarketing Clinical Trial Safety Jul 26, 2014 ACPE, IACET Online Instruction Global Online
    Postmarketing Safety Management Jul 26, 2014 Online Instruction Global Online
    Basics of Signal Detection and Pharmacoepidemiology Jul 26, 2014 Online Instruction Global Online
    Safety Audits and Inspections Jul 26, 2014 Online Instruction Global Online
    Introduction to Drug Safety Jul 26, 2014 ACPE, IACET Online Instruction Global Online
    A Tour of FDA Jul 26, 2014 Online Instruction Global Online
    A Tour of Health Canada Jul 26, 2014 Online Instruction Global Online
    A Tour of Health Europe Jul 26, 2014 Online Instruction Global Online
    Aspects of Regulatory History Jul 26, 2014 Online Instruction Global Online
    Bioresearch Monitoring Program (BIMO): Introduction Jul 26, 2014 Online Instruction Global Online
    The Clinical Development Process: Investigational Product, Plan, and Data Management Jul 26, 2014 Online Instruction Global Online
    Drug Safety & Adverse Event Reporting Jul 26, 2014 Online Instruction Global Online
    Ethical Review Boards Jul 26, 2014 Online Instruction Global Online
    Ethics as the Foundation to Clinical Research Jul 26, 2014 Online Instruction Global Online
    Awareness of FDA Inspections for Pharmaceutical Manufacturers Jul 26, 2014 Online Instruction Global Online
    Biotechnology: An Overview of Compliance Considerations Jul 26, 2014 Online Instruction Global Online
    Change Control Jul 26, 2014 Online Instruction Global Online
    Clinical Trial Audits and Consequences of Non-Compliance Jul 26, 2014 Online Instruction Global Online
    Computerized Systems Inspections in the Medical Device Industry Jul 26, 2014 Online Instruction Global Online
    European Union Clinical Trials Directive Jul 26, 2014 Online Instruction Global Online
    GMP Principals of SOPs Jul 26, 2014 Online Instruction Global Online
    GMP Updates - Enforcement Changes at the New FDA Jul 26, 2014 Online Instruction Global Online
    GMPs for API Bulk Manufacturers Jul 26, 2014 Online Instruction Global Online
    Good Clinical Practices (GCPs) for New Product Investigations Jul 26, 2014 Online Instruction Global Online
    Good Laboratory Practices (GLPs) Jul 26, 2014 Online Instruction Global Online
    GxPs Jul 26, 2014 Online Instruction Global Online
    HIPAA - The Impact on Clinical Research Jul 26, 2014 Online Instruction Global Online
    Introduction to GMPs Jul 26, 2014 Online Instruction Global Online
    Investigational Product Development Jul 26, 2014 Online Instruction Global Online
    ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials Jul 26, 2014 Online Instruction Global Online
    Key Concepts of Process Validation Jul 26, 2014 Online Instruction Global Online
    Laboratory Specimens for Clinical Research Jul 26, 2014 Online Instruction Global Online
    Medical Device Safety Reporting Jul 26, 2014 Online Instruction Global Online
    Orientation to GMP Compliance Jul 26, 2014 Online Instruction Global Online
    Overview of the Clinical Research Process Jul 26, 2014 Online Instruction Global Online
    Part 11: Electronic Records and Signatures - Application Jul 26, 2014 Online Instruction Global Online
    Part 11: Electronic Records; Electronic Signatures Jul 26, 2014 Online Instruction Global Online
    Principles of Good Documentation Jul 26, 2014 Online Instruction Global Online
    Protection of Human Subjects in Clinical Trials Jul 26, 2014 Online Instruction Global Online
    Selecting and Managing Clinical Contract Research Organizations (CROs) Jul 26, 2014 Online Instruction Global Online
    Understanding Post-Approval Changes Jul 26, 2014 Online Instruction Global Online
    Computerized Systems Inspections in the Pharmaceutical Industry Jul 26, 2014 Online Instruction Global Online
    Basics of the PhRMA Code Jul 26, 2014 Online Instruction Global Online
    Basics of AdvaMed Code Jul 26, 2014 Online Instruction Global Online
    Eucomed Guidelines on Interactions with Healthcare Professionals Jul 26, 2014 Online Instruction Global Online
    Introduction to Medical Device Health Care Compliance Jul 26, 2014 Online Instruction Global Online
    Foreign Corrupt Practices Act Jul 26, 2014 Online Instruction Global Online
    Global Anti-bribery Jul 26, 2014 Online Instruction Global Online
    Variations to Marketing Authorisation in Europe Jul 26, 2014 Online Instruction Global Online
    Registration of Monoclonal Antibodies Jul 26, 2014 Online Instruction Global Online
    How to Gain Approval to Market a Generic Medicinal Product in the USA Jul 26, 2014 Online Instruction Global Online
    Pharmacokinetics and Pharmacodynamics in Drug Registration Jul 26, 2014 Online Instruction Global Online
    Introduction to the European Union Institutions and Regulatory Authority Jul 26, 2014 Online Instruction Global Online
    Introduction to US Institutions and Regulatory Authority (FDA) Jul 26, 2014 Online Instruction Global Online
    Introduction to Japanese Institutions and Regulatory Authorities Jul 26, 2014 Online Instruction Global Online
    Overview of the CTD and eCTD Jul 26, 2014 Online Instruction Global Online
    Introduction to the International Conference on Harmonisation (ICH) Jul 26, 2014 Online Instruction Global Online
    The Regulatory Development of a Drug Jul 26, 2014 Online Instruction Global Online
    Basics of Clinical Trials Jul 26, 2014 Online Instruction Global Online
    How to Register Medicinal Products through the Centralized Procedure Jul 26, 2014 Online Instruction Global Online
    How to Register Medicinal Products through the Mutual Recognition Procedure Jul 26, 2014 Online Instruction Global Online
    How to Maintain Marketing Approvals in Europe for Centrally Authorised Products Jul 26, 2014 Online Instruction Global Online
    How to Register a New Drug in the USA Jul 26, 2014 Online Instruction Global Online
    How to Register Medicinal Products through the Decentralized Procedure Jul 26, 2014 Online Instruction Global Online
    Access to Unapproved Drugs through Compassionate Use Jul 26, 2014 Online Instruction Global Online
    Regulatory Requirements for the Conduct of Clinical Trials in Europe Jul 26, 2014 Online Instruction Global Online
    Orphan Drugs in the USA, European Union, and Japan Jul 26, 2014 Online Instruction Global Online
    Regulatory Requirements for the Submission of Investigational New Drug Applications in the USA (INDs) Jul 26, 2014 Online Instruction Global Online
    Meeting Opportunities with Regulatory Agencies Jul 26, 2014 Online Instruction Global Online