DIA
Drug Information Association Logo

Advanced Search

MM-DD-YYYY

Add Filter

    Advanced Search

    Find Meetings & Training 

    Name Start Date Credits Format Region Location
    Clinical Investigator: Module 2 - Conducting the Study Jan 30, 2015 ACPE, CME Online Instruction North America Online
    Clinical Investigator: Module 1 - Study Preparation and Initiation Jan 30, 2015 ACPE, CME Online Instruction North America Online
    Informed Consent Jan 30, 2015 ACPE Online Instruction North America Online
    Crisis Management Jan 30, 2015 ACPE, IACET Online Instruction North America Online
    Database Management Jan 30, 2015 ACPE, IACET Online Instruction North America Online
    Literature Evaluation Jan 30, 2015 ACPE, IACET Online Instruction North America Online
    Literature Searching Jan 30, 2015 ACPE, IACET Online Instruction North America Online
    Medical Inquiries Jan 30, 2015 ACPE, IACET Online Instruction North America Online
    Medical Writing Jan 30, 2015 IACET Online Instruction North America Online
    Product Labeling Jan 30, 2015 ACPE, IACET Online Instruction North America Online
    Regulatory Issues Jan 30, 2015 ACPE, IACET Online Instruction North America Online
    Statistics for Medical Communications Professionals Jan 30, 2015 ACPE, IACET Online Instruction North America Online
    Drug Safety Regulatory Requirements Jan 30, 2015 ACPE, IACET Online Instruction Global Online
    Premarketing Clinical Trial Safety Jan 30, 2015 ACPE, IACET Online Instruction Global Online
    Postmarketing Safety Management Jan 30, 2015 ACPE, IACET Online Instruction Global Online
    Basics of Signal Detection and Pharmacoepidemiology Jan 30, 2015 ACPE, IACET Online Instruction Global Online
    Safety Audits and Inspections Jan 30, 2015 ACPE, IACET Online Instruction Global Online
    Introduction to Drug Safety Jan 30, 2015 ACPE, IACET Online Instruction Global Online
    A Tour of FDA Jan 30, 2015 Online Instruction Global Online
    A Tour of Health Canada Jan 30, 2015 Online Instruction Global Online
    A Tour of Health Europe Jan 30, 2015 Online Instruction Global Online
    Aspects of Regulatory History Jan 30, 2015 Online Instruction Global Online
    Bioresearch Monitoring Program (BIMO): Introduction Jan 30, 2015 Online Instruction Global Online
    The Clinical Development Process: Investigational Product, Plan, and Data Management Jan 30, 2015 Online Instruction Global Online
    Ethical Review Boards Jan 30, 2015 Online Instruction Global Online
    Ethics as the Foundation to Clinical Research Jan 30, 2015 Online Instruction Global Online
    Awareness of FDA Inspections for Pharmaceutical Manufacturers Jan 30, 2015 Online Instruction Global Online
    Biotechnology: An Overview of Compliance Considerations Jan 30, 2015 Online Instruction Global Online
    Change Control Jan 30, 2015 Online Instruction Global Online
    Clinical Trial Audits and Consequences of Non-Compliance Jan 30, 2015 Online Instruction Global Online
    Computerized Systems Inspections in the Medical Device Industry Jan 30, 2015 Online Instruction Global Online
    European Union Clinical Trials Directive Jan 30, 2015 Online Instruction Global Online
    GMP Principals of SOPs Jan 30, 2015 Online Instruction Global Online
    GMP Updates - Enforcement Changes at the New FDA Jan 30, 2015 Online Instruction Global Online
    GMPs for API Bulk Manufacturers Jan 30, 2015 Online Instruction Global Online
    Good Clinical Practices (GCPs) for New Product Investigations Jan 30, 2015 Online Instruction Global Online
    Good Laboratory Practices (GLPs) Jan 30, 2015 Online Instruction Global Online
    GxPs Jan 30, 2015 Online Instruction Global Online
    HIPAA - The Impact on Clinical Research Jan 30, 2015 Online Instruction Global Online
    Introduction to GMPs Jan 30, 2015 Online Instruction Global Online
    Investigational Product Development Jan 30, 2015 Online Instruction Global Online
    ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials Jan 30, 2015 Online Instruction Global Online
    Key Concepts of Process Validation Jan 30, 2015 Online Instruction Global Online
    Laboratory Specimens for Clinical Research Jan 30, 2015 Online Instruction Global Online
    Medical Device Safety Reporting Jan 30, 2015 Online Instruction Global Online
    Orientation to GMP Compliance Jan 30, 2015 Online Instruction Global Online
    Overview of the Clinical Research Process Jan 30, 2015 Online Instruction Global Online
    Part 11: Electronic Records and Signatures - Application Jan 30, 2015 Online Instruction Global Online
    Part 11: Electronic Records; Electronic Signatures Jan 30, 2015 Online Instruction Global Online
    Principles of Good Documentation Jan 30, 2015 Online Instruction Global Online
    Protection of Human Subjects in Clinical Trials Jan 30, 2015 Online Instruction Global Online
    Selecting and Managing Clinical Contract Research Organizations (CROs) Jan 30, 2015 Online Instruction Global Online
    Understanding Post-Approval Changes Jan 30, 2015 Online Instruction Global Online
    Computerized Systems Inspections in the Pharmaceutical Industry Jan 30, 2015 Online Instruction Global Online
    Basics of the PhRMA Code Jan 30, 2015 Online Instruction Global Online
    Basics of AdvaMed Code Jan 30, 2015 Online Instruction Global Online
    Eucomed Guidelines on Interactions with Healthcare Professionals Jan 30, 2015 Online Instruction Global Online
    Introduction to Medical Device Health Care Compliance Jan 30, 2015 Online Instruction Global Online
    Foreign Corrupt Practices Act Jan 30, 2015 Online Instruction Global Online
    Global Anti-bribery Jan 30, 2015 Online Instruction Global Online
    Variations to Marketing Authorisation in Europe Jan 30, 2015 Online Instruction Global Online
    Registration of Monoclonal Antibodies Jan 30, 2015 Online Instruction Global Online
    How to Gain Approval to Market a Generic Medicinal Product in the USA Jan 30, 2015 Online Instruction Global Online
    Pharmacokinetics and Pharmacodynamics in Drug Registration Jan 30, 2015 Online Instruction Global Online
    Introduction to the European Union Institutions and Regulatory Authority Jan 30, 2015 Online Instruction Global Online
    Introduction to US Institutions and Regulatory Authority (FDA) Jan 30, 2015 Online Instruction Global Online
    Introduction to Japanese Institutions and Regulatory Authorities Jan 30, 2015 Online Instruction Global Online
    Overview of the CTD and eCTD Jan 30, 2015 Online Instruction Global Online
    Introduction to the International Conference on Harmonisation (ICH) Jan 30, 2015 Online Instruction Global Online
    The Regulatory Development of a Drug Jan 30, 2015 Online Instruction Global Online
    Basics of Clinical Trials Jan 30, 2015 Online Instruction Global Online
    How to Register Medicinal Products through the Centralized Procedure Jan 30, 2015 Online Instruction Global Online
    How to Register Medicinal Products through the Mutual Recognition Procedure Jan 30, 2015 Online Instruction Global Online
    How to Maintain Marketing Approvals in Europe for Centrally Authorised Products Jan 30, 2015 Online Instruction Global Online
    How to Register a New Drug in the USA Jan 30, 2015 Online Instruction Global Online
    How to Register Medicinal Products through the Decentralized Procedure Jan 30, 2015 Online Instruction Global Online
    Access to Unapproved Drugs through Compassionate Use Jan 30, 2015 Online Instruction Global Online
    Regulatory Requirements for the Conduct of Clinical Trials in Europe Jan 30, 2015 Online Instruction Global Online
    Orphan Drugs in the USA, European Union, and Japan Jan 30, 2015 Online Instruction Global Online
    Regulatory Requirements for the Submission of Investigational New Drug Applications in the USA (INDs) Jan 30, 2015 Online Instruction Global Online
    Meeting Opportunities with Regulatory Agencies Jan 30, 2015 Online Instruction Global Online