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    Name Start Date Credits Format Region Location
    Clinical Investigator: Module 2 - Conducting The Study Oct 20, 2014 ACPE, CME Online Instruction North America Online
    Clinical Investigator: Module 1 - Study Preparation and Initiation Oct 20, 2014 ACPE, CME Online Instruction North America Online
    Informed Consent Oct 20, 2014 ACPE Online Instruction North America Online
    Crisis Management Oct 20, 2014 ACPE, IACET Online Instruction North America Online
    Database Management Oct 20, 2014 ACPE, IACET Online Instruction North America Online
    Literature Evaluation Oct 20, 2014 ACPE, IACET Online Instruction North America Online
    Literature Searching Oct 20, 2014 ACPE, IACET Online Instruction North America Online
    Medical Inquiries Oct 20, 2014 ACPE, IACET Online Instruction North America Online
    Medical Writing Oct 20, 2014 IACET Online Instruction North America Online
    Product Labeling Oct 20, 2014 ACPE, IACET Online Instruction North America Online
    Regulatory Issues Oct 20, 2014 ACPE, IACET Online Instruction North America Online
    Statistics for Medical Communications Professionals Oct 20, 2014 ACPE, IACET Online Instruction North America Online
    Drug Safety Regulatory Requirements Oct 20, 2014 ACPE, IACET Online Instruction Global Online
    Premarketing Clinical Trial Safety Oct 20, 2014 ACPE, IACET Online Instruction Global Online
    Postmarketing Safety Management Oct 20, 2014 ACPE, IACET Online Instruction Global Online
    Basics of Signal Detection and Pharmacoepidemiology Oct 20, 2014 ACPE, IACET Online Instruction Global Online
    Safety Audits and Inspections Oct 20, 2014 Online Instruction Global Online
    Introduction to Drug Safety Oct 20, 2014 ACPE, IACET Online Instruction Global Online
    A Tour of FDA Oct 20, 2014 Online Instruction Global Online
    A Tour of Health Canada Oct 20, 2014 Online Instruction Global Online
    A Tour of Health Europe Oct 20, 2014 Online Instruction Global Online
    Aspects of Regulatory History Oct 20, 2014 Online Instruction Global Online
    Bioresearch Monitoring Program (BIMO): Introduction Oct 20, 2014 Online Instruction Global Online
    The Clinical Development Process: Investigational Product, Plan, and Data Management Oct 20, 2014 Online Instruction Global Online
    Drug Safety & Adverse Event Reporting Oct 20, 2014 Online Instruction Global Online
    Ethical Review Boards Oct 20, 2014 Online Instruction Global Online
    Ethics as the Foundation to Clinical Research Oct 20, 2014 Online Instruction Global Online
    Awareness of FDA Inspections for Pharmaceutical Manufacturers Oct 20, 2014 Online Instruction Global Online
    Biotechnology: An Overview of Compliance Considerations Oct 20, 2014 Online Instruction Global Online
    Change Control Oct 20, 2014 Online Instruction Global Online
    Clinical Trial Audits and Consequences of Non-Compliance Oct 20, 2014 Online Instruction Global Online
    Computerized Systems Inspections in the Medical Device Industry Oct 20, 2014 Online Instruction Global Online
    European Union Clinical Trials Directive Oct 20, 2014 Online Instruction Global Online
    GMP Principals of SOPs Oct 20, 2014 Online Instruction Global Online
    GMP Updates - Enforcement Changes at the New FDA Oct 20, 2014 Online Instruction Global Online
    GMPs for API Bulk Manufacturers Oct 20, 2014 Online Instruction Global Online
    Good Clinical Practices (GCPs) for New Product Investigations Oct 20, 2014 Online Instruction Global Online
    Good Laboratory Practices (GLPs) Oct 20, 2014 Online Instruction Global Online
    GxPs Oct 20, 2014 Online Instruction Global Online
    HIPAA - The Impact on Clinical Research Oct 20, 2014 Online Instruction Global Online
    Introduction to GMPs Oct 20, 2014 Online Instruction Global Online
    Investigational Product Development Oct 20, 2014 Online Instruction Global Online
    ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials Oct 20, 2014 Online Instruction Global Online
    Key Concepts of Process Validation Oct 20, 2014 Online Instruction Global Online
    Laboratory Specimens for Clinical Research Oct 20, 2014 Online Instruction Global Online
    Medical Device Safety Reporting Oct 20, 2014 Online Instruction Global Online
    Orientation to GMP Compliance Oct 20, 2014 Online Instruction Global Online
    Overview of the Clinical Research Process Oct 20, 2014 Online Instruction Global Online
    Part 11: Electronic Records and Signatures - Application Oct 20, 2014 Online Instruction Global Online
    Part 11: Electronic Records; Electronic Signatures Oct 20, 2014 Online Instruction Global Online
    Principles of Good Documentation Oct 20, 2014 Online Instruction Global Online
    Protection of Human Subjects in Clinical Trials Oct 20, 2014 Online Instruction Global Online
    Selecting and Managing Clinical Contract Research Organizations (CROs) Oct 20, 2014 Online Instruction Global Online
    Understanding Post-Approval Changes Oct 20, 2014 Online Instruction Global Online
    Computerized Systems Inspections in the Pharmaceutical Industry Oct 20, 2014 Online Instruction Global Online
    Basics of the PhRMA Code Oct 20, 2014 Online Instruction Global Online
    Basics of AdvaMed Code Oct 20, 2014 Online Instruction Global Online
    Eucomed Guidelines on Interactions with Healthcare Professionals Oct 20, 2014 Online Instruction Global Online
    Introduction to Medical Device Health Care Compliance Oct 20, 2014 Online Instruction Global Online
    Foreign Corrupt Practices Act Oct 20, 2014 Online Instruction Global Online
    Global Anti-bribery Oct 20, 2014 Online Instruction Global Online
    Variations to Marketing Authorisation in Europe Oct 20, 2014 Online Instruction Global Online
    Registration of Monoclonal Antibodies Oct 20, 2014 Online Instruction Global Online
    How to Gain Approval to Market a Generic Medicinal Product in the USA Oct 20, 2014 Online Instruction Global Online
    Pharmacokinetics and Pharmacodynamics in Drug Registration Oct 20, 2014 Online Instruction Global Online
    Introduction to the European Union Institutions and Regulatory Authority Oct 20, 2014 Online Instruction Global Online
    Introduction to US Institutions and Regulatory Authority (FDA) Oct 20, 2014 Online Instruction Global Online
    Introduction to Japanese Institutions and Regulatory Authorities Oct 20, 2014 Online Instruction Global Online
    Overview of the CTD and eCTD Oct 20, 2014 Online Instruction Global Online
    Introduction to the International Conference on Harmonisation (ICH) Oct 20, 2014 Online Instruction Global Online
    The Regulatory Development of a Drug Oct 20, 2014 Online Instruction Global Online
    Basics of Clinical Trials Oct 20, 2014 Online Instruction Global Online
    How to Register Medicinal Products through the Centralized Procedure Oct 20, 2014 Online Instruction Global Online
    How to Register Medicinal Products through the Mutual Recognition Procedure Oct 20, 2014 Online Instruction Global Online
    How to Maintain Marketing Approvals in Europe for Centrally Authorised Products Oct 20, 2014 Online Instruction Global Online
    How to Register a New Drug in the USA Oct 20, 2014 Online Instruction Global Online
    How to Register Medicinal Products through the Decentralized Procedure Oct 20, 2014 Online Instruction Global Online
    Access to Unapproved Drugs through Compassionate Use Oct 20, 2014 Online Instruction Global Online
    Regulatory Requirements for the Conduct of Clinical Trials in Europe Oct 20, 2014 Online Instruction Global Online
    Orphan Drugs in the USA, European Union, and Japan Oct 20, 2014 Online Instruction Global Online
    Regulatory Requirements for the Submission of Investigational New Drug Applications in the USA (INDs) Oct 20, 2014 Online Instruction Global Online
    Meeting Opportunities with Regulatory Agencies Oct 20, 2014 Online Instruction Global Online