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