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    Name Start Date Credits Format Region Location
    Clinical Investigator: Module 2 - Conducting The Study Aug 21, 2014 ACPE, CME Online Instruction North America Online
    Clinical Investigator: Module 1 - Study Preparation and Initiation Aug 21, 2014 ACPE, CME Online Instruction North America Online
    Informed Consent Aug 21, 2014 ACPE Online Instruction North America Online
    Crisis Management Aug 21, 2014 ACPE, IACET Online Instruction North America Online
    Database Management Aug 21, 2014 ACPE, IACET Online Instruction North America Online
    Literature Evaluation Aug 21, 2014 ACPE, IACET Online Instruction North America Online
    Literature Searching Aug 21, 2014 ACPE, IACET Online Instruction North America Online
    Medical Inquiries Aug 21, 2014 ACPE, IACET Online Instruction North America Online
    Medical Writing Aug 21, 2014 IACET Online Instruction North America Online
    Product Labeling Aug 21, 2014 ACPE, IACET Online Instruction North America Online
    Regulatory Issues Aug 21, 2014 ACPE, IACET Online Instruction North America Online
    Statistics for Medical Communications Professionals Aug 21, 2014 ACPE, IACET Online Instruction North America Online
    Drug Safety Regulatory Requirements Aug 21, 2014 ACPE, IACET Online Instruction Global Online
    Premarketing Clinical Trial Safety Aug 21, 2014 ACPE, IACET Online Instruction Global Online
    Postmarketing Safety Management Aug 21, 2014 Online Instruction Global Online
    Basics of Signal Detection and Pharmacoepidemiology Aug 21, 2014 ACPE, IACET Online Instruction Global Online
    Safety Audits and Inspections Aug 21, 2014 Online Instruction Global Online
    Introduction to Drug Safety Aug 21, 2014 ACPE, IACET Online Instruction Global Online
    A Tour of FDA Aug 21, 2014 Online Instruction Global Online
    A Tour of Health Canada Aug 21, 2014 Online Instruction Global Online
    A Tour of Health Europe Aug 21, 2014 Online Instruction Global Online
    Aspects of Regulatory History Aug 21, 2014 Online Instruction Global Online
    Bioresearch Monitoring Program (BIMO): Introduction Aug 21, 2014 Online Instruction Global Online
    The Clinical Development Process: Investigational Product, Plan, and Data Management Aug 21, 2014 Online Instruction Global Online
    Drug Safety & Adverse Event Reporting Aug 21, 2014 Online Instruction Global Online
    Ethical Review Boards Aug 21, 2014 Online Instruction Global Online
    Ethics as the Foundation to Clinical Research Aug 21, 2014 Online Instruction Global Online
    Awareness of FDA Inspections for Pharmaceutical Manufacturers Aug 21, 2014 Online Instruction Global Online
    Biotechnology: An Overview of Compliance Considerations Aug 21, 2014 Online Instruction Global Online
    Change Control Aug 21, 2014 Online Instruction Global Online
    Clinical Trial Audits and Consequences of Non-Compliance Aug 21, 2014 Online Instruction Global Online
    Computerized Systems Inspections in the Medical Device Industry Aug 21, 2014 Online Instruction Global Online
    European Union Clinical Trials Directive Aug 21, 2014 Online Instruction Global Online
    GMP Principals of SOPs Aug 21, 2014 Online Instruction Global Online
    GMP Updates - Enforcement Changes at the New FDA Aug 21, 2014 Online Instruction Global Online
    GMPs for API Bulk Manufacturers Aug 21, 2014 Online Instruction Global Online
    Good Clinical Practices (GCPs) for New Product Investigations Aug 21, 2014 Online Instruction Global Online
    Good Laboratory Practices (GLPs) Aug 21, 2014 Online Instruction Global Online
    GxPs Aug 21, 2014 Online Instruction Global Online
    HIPAA - The Impact on Clinical Research Aug 21, 2014 Online Instruction Global Online
    Introduction to GMPs Aug 21, 2014 Online Instruction Global Online
    Investigational Product Development Aug 21, 2014 Online Instruction Global Online
    ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials Aug 21, 2014 Online Instruction Global Online
    Key Concepts of Process Validation Aug 21, 2014 Online Instruction Global Online
    Laboratory Specimens for Clinical Research Aug 21, 2014 Online Instruction Global Online
    Medical Device Safety Reporting Aug 21, 2014 Online Instruction Global Online
    Orientation to GMP Compliance Aug 21, 2014 Online Instruction Global Online
    Overview of the Clinical Research Process Aug 21, 2014 Online Instruction Global Online
    Part 11: Electronic Records and Signatures - Application Aug 21, 2014 Online Instruction Global Online
    Part 11: Electronic Records; Electronic Signatures Aug 21, 2014 Online Instruction Global Online
    Principles of Good Documentation Aug 21, 2014 Online Instruction Global Online
    Protection of Human Subjects in Clinical Trials Aug 21, 2014 Online Instruction Global Online
    Selecting and Managing Clinical Contract Research Organizations (CROs) Aug 21, 2014 Online Instruction Global Online
    Understanding Post-Approval Changes Aug 21, 2014 Online Instruction Global Online
    Computerized Systems Inspections in the Pharmaceutical Industry Aug 21, 2014 Online Instruction Global Online
    Basics of the PhRMA Code Aug 21, 2014 Online Instruction Global Online
    Basics of AdvaMed Code Aug 21, 2014 Online Instruction Global Online
    Eucomed Guidelines on Interactions with Healthcare Professionals Aug 21, 2014 Online Instruction Global Online
    Introduction to Medical Device Health Care Compliance Aug 21, 2014 Online Instruction Global Online
    Foreign Corrupt Practices Act Aug 21, 2014 Online Instruction Global Online
    Global Anti-bribery Aug 21, 2014 Online Instruction Global Online
    Variations to Marketing Authorisation in Europe Aug 21, 2014 Online Instruction Global Online
    Registration of Monoclonal Antibodies Aug 21, 2014 Online Instruction Global Online
    How to Gain Approval to Market a Generic Medicinal Product in the USA Aug 21, 2014 Online Instruction Global Online
    Pharmacokinetics and Pharmacodynamics in Drug Registration Aug 21, 2014 Online Instruction Global Online
    Introduction to the European Union Institutions and Regulatory Authority Aug 21, 2014 Online Instruction Global Online
    Introduction to US Institutions and Regulatory Authority (FDA) Aug 21, 2014 Online Instruction Global Online
    Introduction to Japanese Institutions and Regulatory Authorities Aug 21, 2014 Online Instruction Global Online
    Overview of the CTD and eCTD Aug 21, 2014 Online Instruction Global Online
    Introduction to the International Conference on Harmonisation (ICH) Aug 21, 2014 Online Instruction Global Online
    The Regulatory Development of a Drug Aug 21, 2014 Online Instruction Global Online
    Basics of Clinical Trials Aug 21, 2014 Online Instruction Global Online
    How to Register Medicinal Products through the Centralized Procedure Aug 21, 2014 Online Instruction Global Online
    How to Register Medicinal Products through the Mutual Recognition Procedure Aug 21, 2014 Online Instruction Global Online
    How to Maintain Marketing Approvals in Europe for Centrally Authorised Products Aug 21, 2014 Online Instruction Global Online
    How to Register a New Drug in the USA Aug 21, 2014 Online Instruction Global Online
    How to Register Medicinal Products through the Decentralized Procedure Aug 21, 2014 Online Instruction Global Online
    Access to Unapproved Drugs through Compassionate Use Aug 21, 2014 Online Instruction Global Online
    Regulatory Requirements for the Conduct of Clinical Trials in Europe Aug 21, 2014 Online Instruction Global Online
    Orphan Drugs in the USA, European Union, and Japan Aug 21, 2014 Online Instruction Global Online
    Regulatory Requirements for the Submission of Investigational New Drug Applications in the USA (INDs) Aug 21, 2014 Online Instruction Global Online
    Meeting Opportunities with Regulatory Agencies Aug 21, 2014 Online Instruction Global Online