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    Name Start Date Credits Format Region Location
    EDM and ERS 2014 Sep 22, 2014 IACET Meetings North America Washington, DC, United States
    Clinical Investigator: Module 2 - Conducting The Study Sep 24, 2014 ACPE, CME Online Instruction North America Online
    Clinical Investigator: Module 1 - Study Preparation and Initiation Sep 24, 2014 ACPE, CME Online Instruction North America Online
    Informed Consent Sep 24, 2014 ACPE Online Instruction North America Online
    Crisis Management Sep 24, 2014 ACPE, IACET Online Instruction North America Online
    Database Management Sep 24, 2014 ACPE, IACET Online Instruction North America Online
    Literature Evaluation Sep 24, 2014 ACPE, IACET Online Instruction North America Online
    Literature Searching Sep 24, 2014 ACPE, IACET Online Instruction North America Online
    Medical Inquiries Sep 24, 2014 ACPE, IACET Online Instruction North America Online
    Medical Writing Sep 24, 2014 IACET Online Instruction North America Online
    Product Labeling Sep 24, 2014 ACPE, IACET Online Instruction North America Online
    Regulatory Issues Sep 24, 2014 ACPE, IACET Online Instruction North America Online
    Statistics for Medical Communications Professionals Sep 24, 2014 ACPE, IACET Online Instruction North America Online
    The Use of Mobile Medical Applications as Companions Sep 24, 2014 Online Instruction Global Online
    Generic Drug Labeling Proposed Rule and Safety Updates Sep 24, 2014 Online Instruction Global Online
    Emerging Technologies to Rare Disorder Drug Development: Promises and Pitfalls Sep 24, 2014 Online Instruction Global Online
    Big Data: Impact of Health Care Reform on Collaborations and Strategies Sep 24, 2014 Online Instruction Global Online
    Implementation of the FDASIA Patient Provisions Sep 24, 2014 Online Instruction Global Online
    Complimentary: Regulatory and Real World Evidence Challenges of Rare Diseases and Orphan Drugs Sep 24, 2014 Online Instruction Global Online
    Variations in the European Union: CMC/Quality Changes Sep 24, 2014 Online Instruction Global Online
    Good Pharmacovigilance Practice: How Good has it Proven to be for Industry? Sep 24, 2014 Online Instruction Global Online
    Pharmacovigilance and Risk Management: Patient Perspective Sep 24, 2014 Online Instruction Global Online
    Complimentary Patient-Centeredness and Engagement in Clinical Research: Opportunities for Industry Sep 24, 2014 Online Instruction Global Online
    Drug Safety Regulatory Requirements Sep 24, 2014 ACPE, IACET Online Instruction Global Online
    Premarketing Clinical Trial Safety Sep 24, 2014 ACPE, IACET Online Instruction Global Online
    Postmarketing Safety Management Sep 24, 2014 ACPE, IACET Online Instruction Global Online
    Basics of Signal Detection and Pharmacoepidemiology Sep 24, 2014 Online Instruction Global Online
    Safety Audits and Inspections Sep 24, 2014 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 1: Fundamentals of Clinical Pharmacology: Pharmacokinetics Sep 24, 2014 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 2: Fundamentals of Clinical Pharmacology: Pharmacodynamics Sep 24, 2014 Online Instruction Global Online
    Pharmacovigilance and Global Harmonization Updates Sep 24, 2014 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology For Drug Development - Part 3: Principles of Modeling and Simulation Sep 24, 2014 Online Instruction Global Online
    Designed for Success: Utilizing Protocol Quality by Design (QbD) to Plan Clinical Studies Sep 24, 2014 Online Instruction Global Online
    Negotiation and Influence Sep 24, 2014 Online Instruction Global Online
    China Update: Regulatory Changes and Implications Sep 24, 2014 Online Instruction Global Online
    Evaluation and Management of Cardiac Conditions in Oncology Patients Sep 24, 2014 Online Instruction Global Online
    Risk Management of Medicinal Products: REMS and RMP - Need for Harmonization Within the ICH Region? Sep 24, 2014 Online Instruction Global Online
    Introduction to Drug Safety Sep 24, 2014 ACPE, IACET Online Instruction Global Online
    How to Prepare for a Safety Inspection Sep 24, 2014 Online Instruction Global Online
    Clinical Statistics for Nonstatisticians Sep 24, 2014 Online Instruction Global Online
    Advanced Clinical Statistics for Nonstatisticians Sep 24, 2014 Online Instruction Global Online
    Development of a Clinical Study Report Sep 24, 2014 Online Instruction Global Online
    Art of Writing a Clinical Overview Sep 24, 2014 Online Instruction Global Online
    CardioVascular Safety: The New Paradigm - Proarrhythmic Assessment of New Drugs without the Thorough QT Study Sep 24, 2014 Online Instruction Global Online
    CardioVascular Safety – What are the Key Issues Regarding Blood Pressure Assessment During Clinical Development Sep 24, 2014 Online Instruction Global Online
    Introductory Principles and Application of Risk Management within Clinical Operations Sep 24, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part VI: Preclinical Toxicology & Safety Sep 24, 2014 Online Instruction Global Online
    Electronic Submissions 101 – Essential MS Word and Adobe Acrobat Tools/Skills and Current IT Options Sep 24, 2014 Online Instruction Global Online
    A Tour of FDA Sep 24, 2014 Online Instruction Global Online
    A Tour of Health Canada Sep 24, 2014 Online Instruction Global Online
    A Tour of Health Europe Sep 24, 2014 Online Instruction Global Online
    Aspects of Regulatory History Sep 24, 2014 Online Instruction Global Online
    Bioresearch Monitoring Program (BIMO): Introduction Sep 24, 2014 Online Instruction Global Online
    The Clinical Development Process: Investigational Product, Plan, and Data Management Sep 24, 2014 Online Instruction Global Online
    Drug Safety & Adverse Event Reporting Sep 24, 2014 Online Instruction Global Online
    Ethical Review Boards Sep 24, 2014 Online Instruction Global Online
    Ethics as the Foundation to Clinical Research Sep 24, 2014 Online Instruction Global Online
    Awareness of FDA Inspections for Pharmaceutical Manufacturers Sep 24, 2014 Online Instruction Global Online
    Biotechnology: An Overview of Compliance Considerations Sep 24, 2014 Online Instruction Global Online
    Change Control Sep 24, 2014 Online Instruction Global Online
    Clinical Trial Audits and Consequences of Non-Compliance Sep 24, 2014 Online Instruction Global Online
    Computerized Systems Inspections in the Medical Device Industry Sep 24, 2014 Online Instruction Global Online
    European Union Clinical Trials Directive Sep 24, 2014 Online Instruction Global Online
    GMP Principals of SOPs Sep 24, 2014 Online Instruction Global Online
    GMP Updates - Enforcement Changes at the New FDA Sep 24, 2014 Online Instruction Global Online
    GMPs for API Bulk Manufacturers Sep 24, 2014 Online Instruction Global Online
    Good Clinical Practices (GCPs) for New Product Investigations Sep 24, 2014 Online Instruction Global Online
    Good Laboratory Practices (GLPs) Sep 24, 2014 Online Instruction Global Online
    GxPs Sep 24, 2014 Online Instruction Global Online
    HIPAA - The Impact on Clinical Research Sep 24, 2014 Online Instruction Global Online
    Introduction to GMPs Sep 24, 2014 Online Instruction Global Online
    Investigational Product Development Sep 24, 2014 Online Instruction Global Online
    ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials Sep 24, 2014 Online Instruction Global Online
    Key Concepts of Process Validation Sep 24, 2014 Online Instruction Global Online
    Laboratory Specimens for Clinical Research Sep 24, 2014 Online Instruction Global Online
    Medical Device Safety Reporting Sep 24, 2014 Online Instruction Global Online
    Orientation to GMP Compliance Sep 24, 2014 Online Instruction Global Online
    Overview of the Clinical Research Process Sep 24, 2014 Online Instruction Global Online
    Part 11: Electronic Records and Signatures - Application Sep 24, 2014 Online Instruction Global Online
    Part 11: Electronic Records; Electronic Signatures Sep 24, 2014 Online Instruction Global Online
    Principles of Good Documentation Sep 24, 2014 Online Instruction Global Online
    Protection of Human Subjects in Clinical Trials Sep 24, 2014 Online Instruction Global Online
    Selecting and Managing Clinical Contract Research Organizations (CROs) Sep 24, 2014 Online Instruction Global Online
    Understanding Post-Approval Changes Sep 24, 2014 Online Instruction Global Online
    Computerized Systems Inspections in the Pharmaceutical Industry Sep 24, 2014 Online Instruction Global Online
    Basics of the PhRMA Code Sep 24, 2014 Online Instruction Global Online
    Basics of AdvaMed Code Sep 24, 2014 Online Instruction Global Online
    Eucomed Guidelines on Interactions with Healthcare Professionals Sep 24, 2014 Online Instruction Global Online
    Introduction to Medical Device Health Care Compliance Sep 24, 2014 Online Instruction Global Online
    Foreign Corrupt Practices Act Sep 24, 2014 Online Instruction Global Online
    Global Anti-bribery Sep 24, 2014 Online Instruction Global Online
    Variations to Marketing Authorisation in Europe Sep 24, 2014 Online Instruction Global Online
    Registration of Monoclonal Antibodies Sep 24, 2014 Online Instruction Global Online
    How to Gain Approval to Market a Generic Medicinal Product in the USA Sep 24, 2014 Online Instruction Global Online
    Pharmacokinetics and Pharmacodynamics in Drug Registration Sep 24, 2014 Online Instruction Global Online
    Complimentary - Planning and Implementing Large Cardiovascular Outcomes Studies: Opportunities & Challenges Sep 24, 2014 Online Instruction Global Online
    Complimentary - Press the Easy Button – Ensure Consistency and Compliance for your Documents through Automation Sep 24, 2014 Online Instruction Global Online
    Complimentary - When Outsourcing Stops Making Sense Sep 24, 2014 Online Instruction Global Online
    Complimentary Quintiles/DIA Webinar - Giving Your Study The Right Start Toward Success Through Optimal Country and Site Selection Sep 24, 2014 Online Instruction Global Online
    Complimentary - Risk-Based Monitoring: Regulatory Expectation and Operational Application Sep 24, 2014 Online Instruction Global Online
    Fundamentals of Project Management for Nonproject Managers Sep 24, 2014 Online Instruction Global Online
    Planning and Managing Your Projects Sep 24, 2014 Online Instruction Global Online
    Change Management, Issues Management, Escalation Management Sep 24, 2014 Online Instruction Global Online
    Project Risk Management: Dealing with the Certainty of Uncertainty Sep 24, 2014 Online Instruction Global Online
    Team Building and Development Sep 24, 2014 Online Instruction Global Online
    Preparing a Clinical Trial Budget Sep 24, 2014 Online Instruction Global Online
    Team Building and Development Sep 24, 2014 Online Instruction Global Online
    Introduction to the European Union Institutions and Regulatory Authority Sep 24, 2014 Online Instruction Global Online
    Introduction to US Institutions and Regulatory Authority (FDA) Sep 24, 2014 Online Instruction Global Online
    Introduction to Japanese Institutions and Regulatory Authorities Sep 24, 2014 Online Instruction Global Online
    Overview of the CTD and eCTD Sep 24, 2014 Online Instruction Global Online
    Introduction to the International Conference on Harmonisation (ICH) Sep 24, 2014 Online Instruction Global Online
    The Regulatory Development of a Drug Sep 24, 2014 Online Instruction Global Online
    Basics of Clinical Trials Sep 24, 2014 Online Instruction Global Online
    How to Register Medicinal Products through the Centralized Procedure Sep 24, 2014 Online Instruction Global Online
    How to Register Medicinal Products through the Mutual Recognition Procedure Sep 24, 2014 Online Instruction Global Online
    How to Maintain Marketing Approvals in Europe for Centrally Authorised Products Sep 24, 2014 Online Instruction Global Online
    How to Register a New Drug in the USA Sep 24, 2014 Online Instruction Global Online
    How to Register Medicinal Products through the Decentralized Procedure Sep 24, 2014 Online Instruction Global Online
    Access to Unapproved Drugs through Compassionate Use Sep 24, 2014 Online Instruction Global Online
    Regulatory Requirements for the Conduct of Clinical Trials in Europe Sep 24, 2014 Online Instruction Global Online
    Orphan Drugs in the USA, European Union, and Japan Sep 24, 2014 Online Instruction Global Online
    Regulatory Requirements for the Submission of Investigational New Drug Applications in the USA (INDs) Sep 24, 2014 Online Instruction Global Online
    Meeting Opportunities with Regulatory Agencies Sep 24, 2014 Online Instruction Global Online
    Combination Products and Convergence: An Overview of Clinical Benefits, Regulatory Issues & Manufacturing Challenges Sep 24, 2014 Online Instruction Global Online
    Clinical Trials Transparency 3-Part Series: Moving the Debate Forward - Realizing the Benefits of Providing Greater Access to Clinical Trial Data: Part 1 - Paving the Way for Greater Access To Data Sep 24, 2014 Online Instruction Global Online
    Strategies for Successfully Introducing REMS to Your Organization: From Development and Implementation and Internal and External Evaluation Sep 24, 2014 Online Instruction Global Online
    The Case of the New England Compounding Center: Learning from the Tragedy Sep 24, 2014 Online Instruction Global Online
    Complimentary - From the Clinic to the CFO: Adaptive Trials and Financial Decision-Making Sep 24, 2014 Online Instruction Global Online
    Adverse Event Reporting Requirements: IND and Postmarketing Sep 24, 2014 Online Instruction Global Online
    Complimentary - The Affiliate Challenge – How to Improve Compliance and Efficiency when Working with Regional Affiliates Sep 24, 2014 Online Instruction Global Online
    The Future of Personalized Medicine and Companion Diagnostics Sep 24, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 1: Overall Challenge: The Vision of Better Medicines for Children Sep 24, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 3: Regulatory Framework EU Sep 24, 2014 Online Instruction Global Online
    Seven-Part Pediatric Drug Development Webinar Series - Part 4: Dosing in Children Sep 24, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 2 Regulatory Framework US Overview Sep 24, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 5: Technical Development: Pediatric Formulations Sep 24, 2014 Online Instruction Global Online
    Basics of the IND Sep 24, 2014 Online Instruction Global Online
    Basics of the NDA Sep 24, 2014 Online Instruction Global Online
    Regulatory Aspects of Prescription Drug/Biologics Advertising and Promotional Labeling Sep 24, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part VII: Operational Challenges of Pediatric Clinical Trials Sep 24, 2014 Online Instruction Global Online
    The Current State of Quality Oversight (QO) in the Pharmaceutical Industry Sep 24, 2014 Online Instruction Global Online
    Supplements and Other Changes to an Approved Application Sep 24, 2014 Online Instruction Global Online
    Introduction to Signal Detection and Data Mining Sep 29, 2014 IACET Online Instruction Global Online
    Pharmacovigilance and Risk Management Planning Oct 01, 2014 ACPE, IACET In-Person Instruction North America Toronto, ON, Canada
    DIA Canadian Pharmacovigilance & Risk Management Oct 02, 2014 IACET Meetings North America Toronto, ON, Canada
    Disruptive Innovation in Medical Information Oct 06, 2014 ACPE, IACET Online Instruction Global Online
    The Role of the Clinical Data Manager Oct 08, 2014 IACET Online Instruction Global Online
    Facets of Drug-Induced Kidney Injury and Regulatory Perspective Oct 08, 2014 ACPE, IACET Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 4: Determining the Safe First Human Dose Oct 09, 2014 ACPE, IACET Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part VII: Operational Challenges of Pediatric Clinical Trials Oct 14, 2014 ACPE, IACET Online Instruction Global Online
    Regulatory Affairs for Biologics Oct 19, 2014 IACET In-Person Instruction North America Irvine, CA, United States
    Postmarketing Drug Safety and Pharmacovigilance Oct 20, 2014 ACPE, IACET In-Person Instruction North America Horsham, PA, United States
    Adaptive Design in Clinical Trials: When and How to Apply Oct 21, 2014 IACET In-Person Instruction North America Philadelphia, PA, United States
    Clinical Trials Transparency 3-Part Series: Moving the Debate Forward-Realizing the Benefits of Providing Greater Access to Clinical Trial Data: Part 2-Connecting the Research Community: Data Sharing–Perspectives from Academia and Patient Advocacy Groups Oct 21, 2014 IACET Online Instruction Global Online
    Complimentary - Moving Your Regulated Content Management Platform to the Cloud: Benefits & Barriers Oct 22, 2014 Online Instruction Global Online
    Biostatistics for Non-Statisticians Oct 27, 2014 IACET In-Person Instruction North America
    Risk Management Plans and Drug Utilization Studies in Canada Oct 27, 2014 IACET In-Person Instruction North America Ottawa, ON, Canada
    DIA’s Annual Canadian Meeting: Thinking Globally, Acting Locally for The Well-Being of the Patient Oct 28, 2014 Meetings North America Ottawa, ON, Canada
    Combination Products: A Comprehensive Overview of Premarket Opportunities and Postmarket Challenges! Oct 28, 2014 IACET In-Person Instruction North America Washington, DC, United States
    Patient Engagement throughout the Full Spectrum of Drug Development: An Interactive Workshop for Life Science Companies and Patient Groups Oct 29, 2014 IACET Meetings North America Washington, DC, United States
    DIA Meeting on Combination Products Oct 29, 2014 IACET Meetings North America Washington, DC, United States
    DIA Meeting on Companion Diagnostics Oct 30, 2014 IACET Meetings North America Washington, DC, United States
    Negotiation and Influence Oct 30, 2014 IACET, PMI Online Instruction Global Online
    Navigating Chemistry, Manufacturing & Controls Through the Drug Development Process Nov 03, 2014 IACET In-Person Instruction North America Horsham, PA, United States
    Advanced Signal Detection - Tools, Triage, Evaluation, and Escalation Nov 03, 2014 IACET In-Person Instruction North America Washington, DC, United States
    From the Pediatric Case Files of FDA Nov 06, 2014 IACET In-Person Instruction North America North Bethesda, MD, United States
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 5: Assessment of QT Prolongation Nov 06, 2014 ACPE, IACET Online Instruction Global Online
    Pediatric Research Conference 2014: Transforming the Pediatric Research Landscape through Innovation and Forward Thinking Nov 06, 2014 IACET Meetings North America North Bethesda, MD, United States
    Electronic Submissions: The Next Era of Electronic Submissions Nov 09, 2014 IACET In-Person Instruction North America Bethesda, MD, United States
    Regulatory Affairs: The IND, NDA, and Postmarketing Nov 10, 2014 IACET In-Person Instruction North America Bethesda, MD, United States
    The Leadership Experience Nov 10, 2014 IACET, PMI In-Person Instruction North America Bethesda, MD, United States
    Risk Management and Safety Communication Strategies Nov 10, 2014 ACPE, IACET In-Person Instruction North America Bethesda, MD, United States
    Optimizing Financial Management to Maximize Clinical Trial Investments Nov 11, 2014 Meetings North America Philadelphia, PA, United States
    Clinical Trials Transparency 3-Part Series: Moving the Debate Forward - Realizing the Benefits of Providing Greater Access to Clinical Trial Data: Part 3 - Understanding the Legislation Landscape: Regulatory Updates from the FDA and EMA Nov 12, 2014 IACET Online Instruction Global Online
    Proarrhythmia Nov 19, 2014 ACPE, IACET Online Instruction Global Online
    Impact on Drug Development of Novel Translational Safety Biomarkers for Improved Detection of Drug-Induced Acute Kidney Injury Nov 20, 2014 ACPE, IACET Online Instruction Global Online
    The Basics of Clinical Data Management From Start to End Dec 03, 2014 IACET In-Person Instruction North America Washington, DC, United States
    Pharmacovigilance and Risk Management Strategies 2015 Jan 26, 2015 Meetings North America Washington, DC, United States
    Joint Adaptive Design and Bayesian Statistics Conference: Drivers of Efficiency in Modern Medical Product Development Feb 10, 2015 Meetings North America Arlington, VA, United States
    Marketing Pharmaceuticals 2015 Feb 17, 2015 Meetings North America Washington, DC, United States
    CMC Workshop 2015 Apr 13, 2015 Meetings North America Bethesda, MD, United States
    DIA/FDA Statistics Forum 2015 Apr 20, 2015 Meetings North America North Bethesda, MD, United States
    DIA 2015 51st Annual Meeting: Develop. Innovate. Advance. Jun 14, 2015 Meetings North America Washington, DC, United States