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