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    Name Start Date Credits Format Region Location
    Clinical Investigator: Module 2 - Conducting The Study Apr 24, 2014 ACPE, CME Online Instruction North America Online
    Clinical Investigator: Module 1 - Study Preparation and Initiation Apr 24, 2014 ACPE, CME Online Instruction North America Online
    Informed Consent Apr 24, 2014 ACPE Online Instruction North America Online
    Crisis Management Apr 24, 2014 ACPE, IACET Online Instruction North America Online
    Database Management Apr 24, 2014 ACPE, IACET Online Instruction North America Online
    Literature Evaluation Apr 24, 2014 ACPE, IACET Online Instruction North America Online
    Literature Searching Apr 24, 2014 ACPE, IACET Online Instruction North America Online
    Medical Inquiries Apr 24, 2014 ACPE, IACET Online Instruction North America Online
    Medical Writing Apr 24, 2014 IACET Online Instruction North America Online
    Product Labeling Apr 24, 2014 ACPE, IACET Online Instruction North America Online
    Regulatory Issues Apr 24, 2014 ACPE, IACET Online Instruction North America Online
    Statistics for Medical Communications Professionals Apr 24, 2014 ACPE, IACET Online Instruction North America Online
    A Tour of FDA Apr 24, 2014 Online Instruction Global Online
    A Tour of Health Canada Apr 24, 2014 Online Instruction Global Online
    A Tour of Health Europe Apr 24, 2014 Online Instruction Global Online
    Aspects of Regulatory History Apr 24, 2014 Online Instruction Global Online
    Bioresearch Monitoring Program (BIMO): Introduction Apr 24, 2014 Online Instruction Global Online
    The Clinical Development Process: Investigational Product, Plan, and Data Management Apr 24, 2014 Online Instruction Global Online
    Drug Safety & Adverse Event Reporting Apr 24, 2014 Online Instruction Global Online
    Ethical Review Boards Apr 24, 2014 Online Instruction Global Online
    Ethics as the Foundation to Clinical Research Apr 24, 2014 Online Instruction Global Online
    Awareness of FDA Inspections for Pharmaceutical Manufacturers Apr 24, 2014 Online Instruction Global Online
    Biotechnology: An Overview of Compliance Considerations Apr 24, 2014 Online Instruction Global Online
    Change Control Apr 24, 2014 Online Instruction Global Online
    Clinical Trial Audits and Consequences of Non-Compliance Apr 24, 2014 Online Instruction Global Online
    Computerized Systems Inspections in the Medical Device Industry Apr 24, 2014 Online Instruction Global Online
    European Union Clinical Trials Directive Apr 24, 2014 Online Instruction Global Online
    GMP Principals of SOPs Apr 24, 2014 Online Instruction Global Online
    GMP Updates - Enforcement Changes at the New FDA Apr 24, 2014 Online Instruction Global Online
    GMPs for API Bulk Manufacturers Apr 24, 2014 Online Instruction Global Online
    Good Clinical Practices (GCPs) for New Product Investigations Apr 24, 2014 Online Instruction Global Online
    Good Laboratory Practices (GLPs) Apr 24, 2014 Online Instruction Global Online
    GxPs Apr 24, 2014 Online Instruction Global Online
    HIPAA - The Impact on Clinical Research Apr 24, 2014 Online Instruction Global Online
    Introduction to GMPs Apr 24, 2014 Online Instruction Global Online
    Investigational Product Development Apr 24, 2014 Online Instruction Global Online
    ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials Apr 24, 2014 Online Instruction Global Online
    Key Concepts of Process Validation Apr 24, 2014 Online Instruction Global Online
    Laboratory Specimens for Clinical Research Apr 24, 2014 Online Instruction Global Online
    Medical Device Safety Reporting Apr 24, 2014 Online Instruction Global Online
    Orientation to GMP Compliance Apr 24, 2014 Online Instruction Global Online
    Overview of the Clinical Research Process Apr 24, 2014 Online Instruction Global Online
    Part 11: Electronic Records and Signatures - Application Apr 24, 2014 Online Instruction Global Online
    Part 11: Electronic Records; Electronic Signatures Apr 24, 2014 Online Instruction Global Online
    Principles of Good Documentation Apr 24, 2014 Online Instruction Global Online
    Protection of Human Subjects in Clinical Trials Apr 24, 2014 Online Instruction Global Online
    Selecting and Managing Clinical Contract Research Organizations (CROs) Apr 24, 2014 Online Instruction Global Online
    Understanding Post-Approval Changes Apr 24, 2014 Online Instruction Global Online
    Computerized Systems Inspections in the Pharmaceutical Industry Apr 24, 2014 Online Instruction Global Online
    Basics of the PhRMA Code Apr 24, 2014 Online Instruction Global Online
    Basics of AdvaMed Code Apr 24, 2014 Online Instruction Global Online
    Eucomed Guidelines on Interactions with Healthcare Professionals Apr 24, 2014 Online Instruction Global Online
    Introduction to Medical Device Health Care Compliance Apr 24, 2014 Online Instruction Global Online
    Foreign Corrupt Practices Act Apr 24, 2014 Online Instruction Global Online
    Global Anti-bribery Apr 24, 2014 Online Instruction Global Online
    Variations to Marketing Authorisation in Europe Apr 24, 2014 Online Instruction Global Online
    Registration of Monoclonal Antibodies Apr 24, 2014 Online Instruction Global Online
    How to Gain Approval to Market a Generic Medicinal Product in the USA Apr 24, 2014 Online Instruction Global Online
    Pharmacokinetics and Pharmacodynamics in Drug Registration Apr 24, 2014 Online Instruction Global Online
    Introduction to the European Union Institutions and Regulatory Authority Apr 24, 2014 Online Instruction Global Online
    Introduction to US Institutions and Regulatory Authority (FDA) Apr 24, 2014 Online Instruction Global Online
    Introduction to Japanese Institutions and Regulatory Authorities Apr 24, 2014 Online Instruction Global Online
    Overview of the CTD and eCTD Apr 24, 2014 Online Instruction Global Online
    Introduction to the International Conference on Harmonisation (ICH) Apr 24, 2014 Online Instruction Global Online
    The Regulatory Development of a Drug Apr 24, 2014 Online Instruction Global Online
    Basics of Clinical Trials Apr 24, 2014 Online Instruction Global Online
    How to Register Medicinal Products through the Centralized Procedure Apr 24, 2014 Online Instruction Global Online
    How to Register Medicinal Products through the Mutual Recognition Procedure Apr 24, 2014 Online Instruction Global Online
    How to Maintain Marketing Approvals in Europe for Centrally Authorised Products Apr 24, 2014 Online Instruction Global Online
    How to Register a New Drug in the USA Apr 24, 2014 Online Instruction Global Online
    How to Register Medicinal Products through the Decentralized Procedure Apr 24, 2014 Online Instruction Global Online
    Access to Unapproved Drugs through Compassionate Use Apr 24, 2014 Online Instruction Global Online
    Regulatory Requirements for the Conduct of Clinical Trials in Europe Apr 24, 2014 Online Instruction Global Online
    Orphan Drugs in the USA, European Union, and Japan Apr 24, 2014 Online Instruction Global Online
    Regulatory Requirements for the Submission of Investigational New Drug Applications in the USA (INDs) Apr 24, 2014 Online Instruction Global Online
    Meeting Opportunities with Regulatory Agencies Apr 24, 2014 Online Instruction Global Online