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    Name Start Date Credits Format Region Location
    Clinical Investigator: Module 2 - Conducting the Study Feb 27, 2015 ACPE, CME Online Instruction North America Online
    Clinical Investigator: Module 1 - Study Preparation and Initiation Feb 27, 2015 ACPE, CME Online Instruction North America Online
    Informed Consent Feb 27, 2015 ACPE Online Instruction North America Online
    Crisis Management Feb 27, 2015 ACPE, IACET Online Instruction North America Online
    Database Management Feb 27, 2015 ACPE, IACET Online Instruction North America Online
    Literature Evaluation Feb 27, 2015 ACPE, IACET Online Instruction North America Online
    Literature Searching Feb 27, 2015 ACPE, IACET Online Instruction North America Online
    Medical Inquiries Feb 27, 2015 ACPE, IACET Online Instruction North America Online
    Medical Writing Feb 27, 2015 IACET Online Instruction North America Online
    Product Labeling Feb 27, 2015 ACPE, IACET Online Instruction North America Online
    Regulatory Issues Feb 27, 2015 ACPE, IACET Online Instruction North America Online
    Statistics for Medical Communications Professionals Feb 27, 2015 ACPE, IACET Online Instruction North America Online
    US Advertising & Promotion Requirements for Promotional Regulatory Compliance: Fundamentals for Marketing Drugs and Devices Feb 27, 2015 Online Instruction Global Online
    US Digital Requirements for Promotional Regulatory Compliance: Fundamentals for Marketing Drugs and Devices Feb 27, 2015 Online Instruction Global Online
    European Advertising & Promotion Requirements for Regulatory Compliance: Comparing Fundamentals for Marketing Drugs in 5 Major European Markets (United Kingdom, Italy, Spain, France, and Germany) Feb 27, 2015 Online Instruction Global Online
    Drug Safety Regulatory Requirements Feb 27, 2015 ACPE, IACET Online Instruction Global Online
    Premarketing Clinical Trial Safety Feb 27, 2015 ACPE, IACET Online Instruction Global Online
    Postmarketing Safety Management Feb 27, 2015 ACPE, IACET Online Instruction Global Online
    Basics of Signal Detection and Pharmacoepidemiology Feb 27, 2015 ACPE, IACET Online Instruction Global Online
    Safety Audits and Inspections Feb 27, 2015 ACPE, IACET Online Instruction Global Online
    Introduction to Drug Safety Feb 27, 2015 ACPE, IACET Online Instruction Global Online
    A Tour of FDA Feb 27, 2015 Online Instruction Global Online
    A Tour of Health Canada Feb 27, 2015 Online Instruction Global Online
    A Tour of Health Europe Feb 27, 2015 Online Instruction Global Online
    Aspects of Regulatory History Feb 27, 2015 Online Instruction Global Online
    Bioresearch Monitoring Program (BIMO): Introduction Feb 27, 2015 Online Instruction Global Online
    The Clinical Development Process: Investigational Product, Plan, and Data Management Feb 27, 2015 Online Instruction Global Online
    Ethical Review Boards Feb 27, 2015 Online Instruction Global Online
    Ethics as the Foundation to Clinical Research Feb 27, 2015 Online Instruction Global Online
    Awareness of FDA Inspections for Pharmaceutical Manufacturers Feb 27, 2015 Online Instruction Global Online
    Biotechnology: An Overview of Compliance Considerations Feb 27, 2015 Online Instruction Global Online
    Change Control Feb 27, 2015 Online Instruction Global Online
    Clinical Trial Audits and Consequences of Non-Compliance Feb 27, 2015 Online Instruction Global Online
    Computerized Systems Inspections in the Medical Device Industry Feb 27, 2015 Online Instruction Global Online
    European Union Clinical Trials Directive Feb 27, 2015 Online Instruction Global Online
    GMP Principals of SOPs Feb 27, 2015 Online Instruction Global Online
    GMP Updates - Enforcement Changes at the New FDA Feb 27, 2015 Online Instruction Global Online
    GMPs for API Bulk Manufacturers Feb 27, 2015 Online Instruction Global Online
    Good Clinical Practices (GCPs) for New Product Investigations Feb 27, 2015 Online Instruction Global Online
    Good Laboratory Practices (GLPs) Feb 27, 2015 Online Instruction Global Online
    GxPs Feb 27, 2015 Online Instruction Global Online
    HIPAA - The Impact on Clinical Research Feb 27, 2015 Online Instruction Global Online
    Introduction to GMPs Feb 27, 2015 Online Instruction Global Online
    Investigational Product Development Feb 27, 2015 Online Instruction Global Online
    ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials Feb 27, 2015 Online Instruction Global Online
    Key Concepts of Process Validation Feb 27, 2015 Online Instruction Global Online
    Laboratory Specimens for Clinical Research Feb 27, 2015 Online Instruction Global Online
    Medical Device Safety Reporting Feb 27, 2015 Online Instruction Global Online
    Orientation to GMP Compliance Feb 27, 2015 Online Instruction Global Online
    Overview of the Clinical Research Process Feb 27, 2015 Online Instruction Global Online
    Part 11: Electronic Records and Signatures - Application Feb 27, 2015 Online Instruction Global Online
    Part 11: Electronic Records; Electronic Signatures Feb 27, 2015 Online Instruction Global Online
    Principles of Good Documentation Feb 27, 2015 Online Instruction Global Online
    Protection of Human Subjects in Clinical Trials Feb 27, 2015 Online Instruction Global Online
    Selecting and Managing Clinical Contract Research Organizations (CROs) Feb 27, 2015 Online Instruction Global Online
    Understanding Post-Approval Changes Feb 27, 2015 Online Instruction Global Online
    Computerized Systems Inspections in the Pharmaceutical Industry Feb 27, 2015 Online Instruction Global Online
    Basics of the PhRMA Code Feb 27, 2015 Online Instruction Global Online
    Basics of AdvaMed Code Feb 27, 2015 Online Instruction Global Online
    Eucomed Guidelines on Interactions with Healthcare Professionals Feb 27, 2015 Online Instruction Global Online
    Introduction to Medical Device Health Care Compliance Feb 27, 2015 Online Instruction Global Online
    Foreign Corrupt Practices Act Feb 27, 2015 Online Instruction Global Online
    Global Anti-bribery Feb 27, 2015 Online Instruction Global Online
    Variations to Marketing Authorisation in Europe Feb 27, 2015 Online Instruction Global Online
    Registration of Monoclonal Antibodies Feb 27, 2015 Online Instruction Global Online
    How to Gain Approval to Market a Generic Medicinal Product in the USA Feb 27, 2015 Online Instruction Global Online
    Pharmacokinetics and Pharmacodynamics in Drug Registration Feb 27, 2015 Online Instruction Global Online
    Introduction to the European Union Institutions and Regulatory Authority Feb 27, 2015 Online Instruction Global Online
    Introduction to US Institutions and Regulatory Authority (FDA) Feb 27, 2015 Online Instruction Global Online
    Introduction to Japanese Institutions and Regulatory Authorities Feb 27, 2015 Online Instruction Global Online
    Overview of the CTD and eCTD Feb 27, 2015 Online Instruction Global Online
    Introduction to the International Conference on Harmonisation (ICH) Feb 27, 2015 Online Instruction Global Online
    The Regulatory Development of a Drug Feb 27, 2015 Online Instruction Global Online
    Basics of Clinical Trials Feb 27, 2015 Online Instruction Global Online
    How to Register Medicinal Products through the Centralized Procedure Feb 27, 2015 Online Instruction Global Online
    How to Register Medicinal Products through the Mutual Recognition Procedure Feb 27, 2015 Online Instruction Global Online
    How to Maintain Marketing Approvals in Europe for Centrally Authorised Products Feb 27, 2015 Online Instruction Global Online
    How to Register a New Drug in the USA Feb 27, 2015 Online Instruction Global Online
    How to Register Medicinal Products through the Decentralized Procedure Feb 27, 2015 Online Instruction Global Online
    Access to Unapproved Drugs through Compassionate Use Feb 27, 2015 Online Instruction Global Online
    Regulatory Requirements for the Conduct of Clinical Trials in Europe Feb 27, 2015 Online Instruction Global Online
    Orphan Drugs in the USA, European Union, and Japan Feb 27, 2015 Online Instruction Global Online
    Regulatory Requirements for the Submission of Investigational New Drug Applications in the USA (INDs) Feb 27, 2015 Online Instruction Global Online
    Meeting Opportunities with Regulatory Agencies Feb 27, 2015 Online Instruction Global Online