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    Name Start Date Credits Format Region Location
    Clinical Investigator: Module 2 - Conducting The Study Sep 30, 2014 ACPE, CME Online Instruction North America Online
    Clinical Investigator: Module 1 - Study Preparation and Initiation Sep 30, 2014 ACPE, CME Online Instruction North America Online
    Informed Consent Sep 30, 2014 ACPE Online Instruction North America Online
    Crisis Management Sep 30, 2014 ACPE, IACET Online Instruction North America Online
    Database Management Sep 30, 2014 ACPE, IACET Online Instruction North America Online
    Literature Evaluation Sep 30, 2014 ACPE, IACET Online Instruction North America Online
    Literature Searching Sep 30, 2014 ACPE, IACET Online Instruction North America Online
    Medical Inquiries Sep 30, 2014 ACPE, IACET Online Instruction North America Online
    Medical Writing Sep 30, 2014 IACET Online Instruction North America Online
    Product Labeling Sep 30, 2014 ACPE, IACET Online Instruction North America Online
    Regulatory Issues Sep 30, 2014 ACPE, IACET Online Instruction North America Online
    Statistics for Medical Communications Professionals Sep 30, 2014 ACPE, IACET Online Instruction North America Online
    Drug Safety Regulatory Requirements Sep 30, 2014 ACPE, IACET Online Instruction Global Online
    Premarketing Clinical Trial Safety Sep 30, 2014 ACPE, IACET Online Instruction Global Online
    Postmarketing Safety Management Sep 30, 2014 ACPE, IACET Online Instruction Global Online
    Basics of Signal Detection and Pharmacoepidemiology Sep 30, 2014 ACPE, IACET Online Instruction Global Online
    Safety Audits and Inspections Sep 30, 2014 Online Instruction Global Online
    Introduction to Drug Safety Sep 30, 2014 ACPE, IACET Online Instruction Global Online
    A Tour of FDA Sep 30, 2014 Online Instruction Global Online
    A Tour of Health Canada Sep 30, 2014 Online Instruction Global Online
    A Tour of Health Europe Sep 30, 2014 Online Instruction Global Online
    Aspects of Regulatory History Sep 30, 2014 Online Instruction Global Online
    Bioresearch Monitoring Program (BIMO): Introduction Sep 30, 2014 Online Instruction Global Online
    The Clinical Development Process: Investigational Product, Plan, and Data Management Sep 30, 2014 Online Instruction Global Online
    Drug Safety & Adverse Event Reporting Sep 30, 2014 Online Instruction Global Online
    Ethical Review Boards Sep 30, 2014 Online Instruction Global Online
    Ethics as the Foundation to Clinical Research Sep 30, 2014 Online Instruction Global Online
    Awareness of FDA Inspections for Pharmaceutical Manufacturers Sep 30, 2014 Online Instruction Global Online
    Biotechnology: An Overview of Compliance Considerations Sep 30, 2014 Online Instruction Global Online
    Change Control Sep 30, 2014 Online Instruction Global Online
    Clinical Trial Audits and Consequences of Non-Compliance Sep 30, 2014 Online Instruction Global Online
    Computerized Systems Inspections in the Medical Device Industry Sep 30, 2014 Online Instruction Global Online
    European Union Clinical Trials Directive Sep 30, 2014 Online Instruction Global Online
    GMP Principals of SOPs Sep 30, 2014 Online Instruction Global Online
    GMP Updates - Enforcement Changes at the New FDA Sep 30, 2014 Online Instruction Global Online
    GMPs for API Bulk Manufacturers Sep 30, 2014 Online Instruction Global Online
    Good Clinical Practices (GCPs) for New Product Investigations Sep 30, 2014 Online Instruction Global Online
    Good Laboratory Practices (GLPs) Sep 30, 2014 Online Instruction Global Online
    GxPs Sep 30, 2014 Online Instruction Global Online
    HIPAA - The Impact on Clinical Research Sep 30, 2014 Online Instruction Global Online
    Introduction to GMPs Sep 30, 2014 Online Instruction Global Online
    Investigational Product Development Sep 30, 2014 Online Instruction Global Online
    ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials Sep 30, 2014 Online Instruction Global Online
    Key Concepts of Process Validation Sep 30, 2014 Online Instruction Global Online
    Laboratory Specimens for Clinical Research Sep 30, 2014 Online Instruction Global Online
    Medical Device Safety Reporting Sep 30, 2014 Online Instruction Global Online
    Orientation to GMP Compliance Sep 30, 2014 Online Instruction Global Online
    Overview of the Clinical Research Process Sep 30, 2014 Online Instruction Global Online
    Part 11: Electronic Records and Signatures - Application Sep 30, 2014 Online Instruction Global Online
    Part 11: Electronic Records; Electronic Signatures Sep 30, 2014 Online Instruction Global Online
    Principles of Good Documentation Sep 30, 2014 Online Instruction Global Online
    Protection of Human Subjects in Clinical Trials Sep 30, 2014 Online Instruction Global Online
    Selecting and Managing Clinical Contract Research Organizations (CROs) Sep 30, 2014 Online Instruction Global Online
    Understanding Post-Approval Changes Sep 30, 2014 Online Instruction Global Online
    Computerized Systems Inspections in the Pharmaceutical Industry Sep 30, 2014 Online Instruction Global Online
    Basics of the PhRMA Code Sep 30, 2014 Online Instruction Global Online
    Basics of AdvaMed Code Sep 30, 2014 Online Instruction Global Online
    Eucomed Guidelines on Interactions with Healthcare Professionals Sep 30, 2014 Online Instruction Global Online
    Introduction to Medical Device Health Care Compliance Sep 30, 2014 Online Instruction Global Online
    Foreign Corrupt Practices Act Sep 30, 2014 Online Instruction Global Online
    Global Anti-bribery Sep 30, 2014 Online Instruction Global Online
    Variations to Marketing Authorisation in Europe Sep 30, 2014 Online Instruction Global Online
    Registration of Monoclonal Antibodies Sep 30, 2014 Online Instruction Global Online
    How to Gain Approval to Market a Generic Medicinal Product in the USA Sep 30, 2014 Online Instruction Global Online
    Pharmacokinetics and Pharmacodynamics in Drug Registration Sep 30, 2014 Online Instruction Global Online
    Introduction to the European Union Institutions and Regulatory Authority Sep 30, 2014 Online Instruction Global Online
    Introduction to US Institutions and Regulatory Authority (FDA) Sep 30, 2014 Online Instruction Global Online
    Introduction to Japanese Institutions and Regulatory Authorities Sep 30, 2014 Online Instruction Global Online
    Overview of the CTD and eCTD Sep 30, 2014 Online Instruction Global Online
    Introduction to the International Conference on Harmonisation (ICH) Sep 30, 2014 Online Instruction Global Online
    The Regulatory Development of a Drug Sep 30, 2014 Online Instruction Global Online
    Basics of Clinical Trials Sep 30, 2014 Online Instruction Global Online
    How to Register Medicinal Products through the Centralized Procedure Sep 30, 2014 Online Instruction Global Online
    How to Register Medicinal Products through the Mutual Recognition Procedure Sep 30, 2014 Online Instruction Global Online
    How to Maintain Marketing Approvals in Europe for Centrally Authorised Products Sep 30, 2014 Online Instruction Global Online
    How to Register a New Drug in the USA Sep 30, 2014 Online Instruction Global Online
    How to Register Medicinal Products through the Decentralized Procedure Sep 30, 2014 Online Instruction Global Online
    Access to Unapproved Drugs through Compassionate Use Sep 30, 2014 Online Instruction Global Online
    Regulatory Requirements for the Conduct of Clinical Trials in Europe Sep 30, 2014 Online Instruction Global Online
    Orphan Drugs in the USA, European Union, and Japan Sep 30, 2014 Online Instruction Global Online
    Regulatory Requirements for the Submission of Investigational New Drug Applications in the USA (INDs) Sep 30, 2014 Online Instruction Global Online
    Meeting Opportunities with Regulatory Agencies Sep 30, 2014 Online Instruction Global Online