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    Name Start Date Credits Format Region Location
    A Model of Patient, Payer, and Product Developer Collaboration to Support Innovating for Value - CANCELLED Apr 22, 2014 Meetings North America Washington, DC, United States
    Clinical Investigator: Module 2 - Conducting The Study Apr 23, 2014 ACPE, CME Online Instruction North America Online
    Clinical Investigator: Module 1 - Study Preparation and Initiation Apr 23, 2014 ACPE, CME Online Instruction North America Online
    Informed Consent Apr 23, 2014 ACPE Online Instruction North America Online
    Crisis Management Apr 23, 2014 ACPE, IACET Online Instruction North America Online
    Database Management Apr 23, 2014 ACPE, IACET Online Instruction North America Online
    Literature Evaluation Apr 23, 2014 ACPE, IACET Online Instruction North America Online
    Literature Searching Apr 23, 2014 ACPE, IACET Online Instruction North America Online
    Medical Inquiries Apr 23, 2014 ACPE, IACET Online Instruction North America Online
    Medical Writing Apr 23, 2014 IACET Online Instruction North America Online
    Product Labeling Apr 23, 2014 ACPE, IACET Online Instruction North America Online
    Regulatory Issues Apr 23, 2014 ACPE, IACET Online Instruction North America Online
    Statistics for Medical Communications Professionals Apr 23, 2014 ACPE, IACET Online Instruction North America Online
    The Use of Mobile Medical Applications as Companions Apr 23, 2014 Online Instruction Global Online
    Regulating a Social World Apr 23, 2014 Online Instruction Global Online
    English Literacy and Spanish Transcreation of Patient Documents: Concepts for Low Literacy Materials Apr 23, 2014 Online Instruction Global Online
    Emerging Technologies to Rare Disorder Drug Development: Promises and Pitfalls Apr 23, 2014 Online Instruction Global Online
    Implementation of the FDASIA Patient Provisions Apr 23, 2014 Online Instruction Global Online
    Safety and Social Media: Is this the Question or the Answer Apr 23, 2014 Online Instruction Global Online
    Complimentary Patient-Centeredness and Engagement in Clinical Research: Opportunities for Industry Apr 23, 2014 Online Instruction Global Online
    Aligning the Voices of Change in the Health Care System Apr 23, 2014 Online Instruction Global Online
    Negotiation and Influence Apr 23, 2014 Online Instruction Global Online
    Evaluation and Management of Cardiac Conditions in Oncology Patients Apr 23, 2014 Online Instruction Global Online
    Risk Management of Medicinal Products: REMS and RMP - Need for Harmonization Within the ICH Region? Apr 23, 2014 Online Instruction Global Online
    A Closer Look at FDASIA Provisions to Promote Biomedical Innovation Apr 23, 2014 Online Instruction Global Online
    CDER Town Meeting: Safety Hot Topics Apr 23, 2014 Online Instruction Global Online
    Assessing the Benefits and Risks of Medicines: Webinar Series - Part 1: Introduction to the Benefit-Risk - Why is Everyone Talking about Benefit-Risk? Apr 23, 2014 Online Instruction Global Online
    Assessing the Benefits and Risks of Medicines: Webinar Series Part 2 - Benefit-Risk Assessment a Changing Regulatory Landscape Apr 23, 2014 Online Instruction Global Online
    Assessing the Benefits and Risks of Medicines: Webinar Series - Part 3: Framing for Benefit-Risk Assessment and Communication Apr 23, 2014 Online Instruction Global Online
    Assessing the Benefits and Risks of Medicines: Webinar Series - Part 4: Clinical Judgment and Pragmatic Considerations for Endpoint Selection and Display in Benefit-Risk Apr 23, 2014 Online Instruction Global Online
    Assessing the Benefits and Risks of Medicines: Webinar Series- Part 5: Stated Choice Methods for Valuing Benefits and Risks Apr 23, 2014 Online Instruction Global Online
    Assessing the Benefits and Risks of Medicines: Webinar Series-Part 6: Multi-criteria Decision Analysis to Assist in the Decision Making Process Apr 23, 2014 Online Instruction Global Online
    Assessing the Benefits and Risks of Medicines: Webinar Series- Part 7: A Structured, Quantitative Health Outcomes Approach to Drug Benefit-Risk Analysis Apr 23, 2014 Online Instruction Global Online
    Assessing the Benefits and Risks of Medicines: Webinar Series- Part 8: Visualization and Communication of Benefit-Risk Apr 23, 2014 Online Instruction Global Online
    Practical Aspects and Examples of Using Large Datasets for Investigating Product Safety and Effectiveness in the US and EU Apr 23, 2014 Online Instruction Global Online
    New Good Pharmacovigilance Practice (GVP) Documents in Canada Apr 23, 2014 Online Instruction Global Online
    Clinical Statistics for Nonstatisticians Apr 23, 2014 Online Instruction Global Online
    Development of a Clinical Study Report Apr 23, 2014 Online Instruction Global Online
    Complimentary Biomarker Strategies for More Efficient Early-Phase Drug Development in Alzheimer's Disease Apr 23, 2014 Online Instruction Global Online
    Using Patient-Reported Outcomes to Assess Product Safety and Tolerability: Methodological and Regulatory Considerations Apr 23, 2014 Online Instruction Global Online
    CardioVascular Safety: The New Paradigm - Proarrhythmic Assessment of New Drugs without the Thorough QT Study Apr 23, 2014 Online Instruction Global Online
    CardioVascular Safety – What are the Key Issues Regarding Blood Pressure Assessment During Clinical Development Apr 23, 2014 Online Instruction Global Online
    Electronic Submissions 101 – Essential MS Word and Adobe Acrobat Tools/Skills and Current IT Options Apr 23, 2014 Online Instruction Global Online
    EDM and ERS/eCTD: Impact of e-Initiatives on Content and Context: FDA Update/Progress Report Apr 23, 2014 Online Instruction Global Online
    Regulatory and Legal Landscape Impacting Medical and Scientific Communications Apr 23, 2014 Online Instruction Global Online
    A Tour of FDA Apr 23, 2014 Online Instruction Global Online
    A Tour of Health Canada Apr 23, 2014 Online Instruction Global Online
    A Tour of Health Europe Apr 23, 2014 Online Instruction Global Online
    Aspects of Regulatory History Apr 23, 2014 Online Instruction Global Online
    Bioresearch Monitoring Program (BIMO): Introduction Apr 23, 2014 Online Instruction Global Online
    The Clinical Development Process: Investigational Product, Plan, and Data Management Apr 23, 2014 Online Instruction Global Online
    Drug Safety & Adverse Event Reporting Apr 23, 2014 Online Instruction Global Online
    Ethical Review Boards Apr 23, 2014 Online Instruction Global Online
    Ethics as the Foundation to Clinical Research Apr 23, 2014 Online Instruction Global Online
    Awareness of FDA Inspections for Pharmaceutical Manufacturers Apr 23, 2014 Online Instruction Global Online
    Biotechnology: An Overview of Compliance Considerations Apr 23, 2014 Online Instruction Global Online
    Change Control Apr 23, 2014 Online Instruction Global Online
    Clinical Trial Audits and Consequences of Non-Compliance Apr 23, 2014 Online Instruction Global Online
    Computerized Systems Inspections in the Medical Device Industry Apr 23, 2014 Online Instruction Global Online
    European Union Clinical Trials Directive Apr 23, 2014 Online Instruction Global Online
    GMP Principals of SOPs Apr 23, 2014 Online Instruction Global Online
    GMP Updates - Enforcement Changes at the New FDA Apr 23, 2014 Online Instruction Global Online
    GMPs for API Bulk Manufacturers Apr 23, 2014 Online Instruction Global Online
    Good Clinical Practices (GCPs) for New Product Investigations Apr 23, 2014 Online Instruction Global Online
    Good Laboratory Practices (GLPs) Apr 23, 2014 Online Instruction Global Online
    GxPs Apr 23, 2014 Online Instruction Global Online
    HIPAA - The Impact on Clinical Research Apr 23, 2014 Online Instruction Global Online
    Introduction to GMPs Apr 23, 2014 Online Instruction Global Online
    Investigational Product Development Apr 23, 2014 Online Instruction Global Online
    ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials Apr 23, 2014 Online Instruction Global Online
    Key Concepts of Process Validation Apr 23, 2014 Online Instruction Global Online
    Laboratory Specimens for Clinical Research Apr 23, 2014 Online Instruction Global Online
    Medical Device Safety Reporting Apr 23, 2014 Online Instruction Global Online
    Orientation to GMP Compliance Apr 23, 2014 Online Instruction Global Online
    Overview of the Clinical Research Process Apr 23, 2014 Online Instruction Global Online
    Part 11: Electronic Records and Signatures - Application Apr 23, 2014 Online Instruction Global Online
    Part 11: Electronic Records; Electronic Signatures Apr 23, 2014 Online Instruction Global Online
    Principles of Good Documentation Apr 23, 2014 Online Instruction Global Online
    Protection of Human Subjects in Clinical Trials Apr 23, 2014 Online Instruction Global Online
    Selecting and Managing Clinical Contract Research Organizations (CROs) Apr 23, 2014 Online Instruction Global Online
    Understanding Post-Approval Changes Apr 23, 2014 Online Instruction Global Online
    Computerized Systems Inspections in the Pharmaceutical Industry Apr 23, 2014 Online Instruction Global Online
    Basics of the PhRMA Code Apr 23, 2014 Online Instruction Global Online
    Basics of AdvaMed Code Apr 23, 2014 Online Instruction Global Online
    Eucomed Guidelines on Interactions with Healthcare Professionals Apr 23, 2014 Online Instruction Global Online
    Introduction to Medical Device Health Care Compliance Apr 23, 2014 Online Instruction Global Online
    Foreign Corrupt Practices Act Apr 23, 2014 Online Instruction Global Online
    Global Anti-bribery Apr 23, 2014 Online Instruction Global Online
    Variations to Marketing Authorisation in Europe Apr 23, 2014 Online Instruction Global Online
    Registration of Monoclonal Antibodies Apr 23, 2014 Online Instruction Global Online
    How to Gain Approval to Market a Generic Medicinal Product in the USA Apr 23, 2014 Online Instruction Global Online
    Pharmacokinetics and Pharmacodynamics in Drug Registration Apr 23, 2014 Online Instruction Global Online
    Measurement in Clinical Trials: An Examination of the FDA Position on Review of Clinical Outcome Assessments (COAs) Apr 23, 2014 Online Instruction Global Online
    The Electronic Trial Master File: So Much More than Just a Secure Document Repository Apr 23, 2014 Online Instruction Global Online
    Planning and Implementing Large Cardiovascular Outcomes Studies: Opportunities & Challenges Apr 23, 2014 Online Instruction Global Online
    Press the Easy Button – Ensure Consistency and Compliance for your Documents through Automation Apr 23, 2014 Online Instruction Global Online
    When Outsourcing Stops Making Sense Apr 23, 2014 Online Instruction Global Online
    Complimentary Quintiles/DIA Webinar - Giving Your Study The Right Start Toward Success Through Optimal Country and Site Selection Apr 23, 2014 Online Instruction Global Online
    Fundamentals of Project Management for Nonproject Managers Apr 23, 2014 Online Instruction Global Online
    Planning and Managing Your Project Apr 23, 2014 Online Instruction Global Online
    Change Management, Issues Management, Escalation Management Apr 23, 2014 Online Instruction Global Online
    Preparing a Clinical Trial Budget Apr 23, 2014 Online Instruction Global Online
    Project Risk Management: Dealing with the Certainty of Uncertainty Apr 23, 2014 Online Instruction Global Online
    Team Building and Development Apr 23, 2014 Online Instruction Global Online
    Drug & Cosmetic Rule Amendments: Changes in Regulations Governing Clinical Trials in India Apr 23, 2014 Online Instruction Global Online
    Introduction to the European Union Institutions and Regulatory Authority Apr 23, 2014 Online Instruction Global Online
    Introduction to US Institutions and Regulatory Authority (FDA) Apr 23, 2014 Online Instruction Global Online
    Introduction to Japanese Institutions and Regulatory Authorities Apr 23, 2014 Online Instruction Global Online
    Overview of the CTD and eCTD Apr 23, 2014 Online Instruction Global Online
    Introduction to the International Conference on Harmonisation (ICH) Apr 23, 2014 Online Instruction Global Online
    The Regulatory Development of a Drug Apr 23, 2014 Online Instruction Global Online
    Basics of Clinical Trials Apr 23, 2014 Online Instruction Global Online
    How to Register Medicinal Products through the Centralized Procedure Apr 23, 2014 Online Instruction Global Online
    How to Register Medicinal Products through the Mutual Recognition Procedure Apr 23, 2014 Online Instruction Global Online
    How to Maintain Marketing Approvals in Europe for Centrally Authorised Products Apr 23, 2014 Online Instruction Global Online
    How to Register a New Drug in the USA Apr 23, 2014 Online Instruction Global Online
    How to Register Medicinal Products through the Decentralized Procedure Apr 23, 2014 Online Instruction Global Online
    Access to Unapproved Drugs through Compassionate Use Apr 23, 2014 Online Instruction Global Online
    Regulatory Requirements for the Conduct of Clinical Trials in Europe Apr 23, 2014 Online Instruction Global Online
    Orphan Drugs in the USA, European Union, and Japan Apr 23, 2014 Online Instruction Global Online
    Regulatory Requirements for the Submission of Investigational New Drug Applications in the USA (INDs) Apr 23, 2014 Online Instruction Global Online
    Meeting Opportunities with Regulatory Agencies Apr 23, 2014 Online Instruction Global Online
    A Regulatory Perspective of Biosimilars in Emerging Markets Apr 23, 2014 Online Instruction Global Online
    Combination Products and Convergence: An Overview of Clinical Benefits, Regulatory Issues & Manufacturing Challenges Apr 23, 2014 Online Instruction Global Online
    Social and Collaborative Tools in Regulatory Intelligence Apr 23, 2014 Online Instruction Global Online
    Certificates of Pharmaceutical Products for Regulatory Submissions Apr 23, 2014 Online Instruction Global Online
    FDASIA Year in Review Apr 23, 2014 Online Instruction Global Online
    The Case of the New England Compounding Center: Learning from the Tragedy Apr 23, 2014 Online Instruction Global Online
    The Future of Personalized Medicine and Companion Diagnostics Apr 23, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 1: Overall Challenge: The Vision of Better Medicines for Children Apr 23, 2014 Online Instruction Global Online
    Two-part Webinar Series: Impact of the New European Pharmacovigilance Legislation and Important Updates Apr 23, 2014 Online Instruction Global Online
    FDA and the Freedom of Information Act: The Unredacted Story Apr 23, 2014 Online Instruction Global Online
    The Current State of Quality Oversight (QO) in the Pharmaceutical Industry Apr 23, 2014 Online Instruction Global Online
    Combination Product Premarket Considerations Apr 23, 2014 Online Instruction Global Online
    Utilizing the 505(b)(2) Pathway to Streamline and Accelerate a Drug Development Plan Apr 23, 2014 Online Instruction Global Online
    Strategies for Successfully Introducing REMS to Your Organization: From Development and Implementation to Internal and External Evaluation Apr 23, 2014 IACET Online Instruction Global Online
    Good Pharmacovigilance Practice: How Good has it Proven to be for Industry? Apr 29, 2014 IACET Online Instruction Global Online
    Basics of the IND Apr 29, 2014 IACET Online Instruction Global Online
    Designed for Success: Utilizing Protocol Quality by Design (QbD) to Plan Clinical Studies May 01, 2014 IACET Online Instruction Global Online
    Global Considerations for Regulatory Strategy Development May 05, 2014 IACET In-Person Instruction North America Horsham, PA, United States
    How to Prepare for a Safety Inspection May 06, 2014 IACET Online Instruction Global Online
    Drug-Induced Injury of Liver, Heart, Kidney, and Skin: Employing Recent Advances to Improve Patient Safety and Speed Up the Pipeline May 07, 2014 ACPE, CME, IACET Meetings North America North Bethesda, MD, United States
    Oversight of Clinical Monitoring: Trends and Strategies May 13, 2014 IACET Online Instruction Global Online
    Generic Drug Labeling Proposed Rule and Safety Updates May 15, 2014 Online Instruction Global Online
    Complimentary DIA/Covance Webinar - Risk-Based Monitoring: Regulatory Expectation and Operational Application May 15, 2014 Online Instruction Global Online
    Big Data: Impact of Health Care Reform on Collaborations and Strategies May 19, 2014 IACET Online Instruction Global Online
    Biostatistics and FDA Regulation: The Convergence of Science and Law May 20, 2014 Meetings North America Cambridge, MA, United States
    Seven-Part Series on Pediatric Drug Development - Part 2: Regulatory Framework, US May 20, 2014 ACPE, IACET Online Instruction Global Online
    Basics of the NDA May 20, 2014 IACET Online Instruction Global Online
    Pharmacovigilance and Risk Management: Patient Perspective May 22, 2014 Online Instruction Global Online
    China Update: Regulatory Changes and Implications May 28, 2014 Online Instruction Global Online
    Complimentary DIA/Optum Webinar: Regulatory and Real World Evidence Challenges of Rare Diseases and Orphan Drugs May 28, 2014 Online Instruction Global Online
    Preparing for a Clinical Trial Budget Jun 03, 2014 IACET, PMI Online Instruction Global Online
    Regulatory Aspects of Prescription Drug/Biologics Advertising and Promotional Labeling Jun 05, 2014 IACET Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 3: Regulatory Framework EU Jun 10, 2014 ACPE, IACET Online Instruction Global Online
    Supplements and Other Changes to an Approved Application Jun 10, 2014 IACET Online Instruction Global Online
    #20: Japan Regulatory Environment: Overview of the Organization, Processes, Systems, and Changes Affecting Pharmaceutical Development Jun 15, 2014 IACET In-Person Instruction North America San Diego, CA, United States
    #21: The Sunshine Act: Understanding the Essentials of Compliance Jun 15, 2014 CME, IACET, RN In-Person Instruction North America San Diego, CA, United States
    #22: Preparing for a US FDA Advisory Committee Meeting Jun 15, 2014 IACET In-Person Instruction North America San Diego, CA, United States
    #23: Leadership: How to Organize and Lead People in Group Work Jun 15, 2014 IACET, PMI In-Person Instruction North America San Diego, CA, United States
    #24: Successful Drug Development: Best Practices for Clinical Trial Design, Agency Interactions, and Regulatory Document Writing Jun 15, 2014 IACET In-Person Instruction North America San Diego, CA, United States
    DIA 2014 50th Annual Meeting 'Celebrate the Past - Invent the Future' Jun 15, 2014 Meetings North America San Diego, CA, United States
    #40: Analysis of Safety Data from Clinical Trials Jun 15, 2014 ACPE, CME, IACET, RN In-Person Instruction North America San Diego, CA, United States
    #41: Quality Oversight of CROs-Clinical Vendors Jun 15, 2014 IACET In-Person Instruction North America San Diego, CA, United States
    #42: Regulatory Affairs for Biologics Jun 15, 2014 IACET In-Person Instruction North America San Diego, CA, United States
    #43: Clinical Statistics for Nonstatisticians Jun 15, 2014 ACPE, CME, IACET, RN In-Person Instruction North America San Diego, CA, United States
    #44: Quality by Design: From Theory to Practice Jun 15, 2014 CME, IACET, RN In-Person Instruction North America San Diego, CA, United States
    #45: Risk Management Plan Jun 15, 2014 ACPE, CME, IACET, RN In-Person Instruction North America San Diego, CA, United States
    #46: The Good Pharmacovigilance Practices In The EU: Lessons Learned and Frequently Asked Implementation Questions Jun 15, 2014 CME, IACET, RN In-Person Instruction North America San Diego, CA, United States
    #30: Influencing Culture, Avoiding Bureaucracy, and Encouraging Innovation Jun 15, 2014 IACET In-Person Instruction North America San Diego, CA, United States
    #31: Large-Scale Regulatory Functional Outsourcing: Emerging Trends, Challenges and Decision Criteria Jun 15, 2014 IACET In-Person Instruction North America San Diego, CA, United States
    #32: Pharmacogenomics and Companion Diagnostics: The Future of Clinical Trials, New Product Development and the Practice of Medicine Jun 15, 2014 ACPE, CME, IACET, RN In-Person Instruction North America San Diego, CA, United States
    #33: Bayesian Evidence Synthesis and Network Meta-analysis Jun 15, 2014 CME, IACET, RN In-Person Instruction North America San Diego, CA, United States
    #34: Preparation of Risk Evaluation and Mitigation Strategies Assessment Reports Jun 15, 2014 ACPE, CME, IACET, RN In-Person Instruction North America San Diego, CA, United States
    #35: Understanding Translational Medicine: Benefits and Innovative Approaches Jun 15, 2014 CME, IACET, RN In-Person Instruction North America San Diego, CA, United States
    Variations in the European Union: CMC/Quality Changes Jun 26, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 4: Dosing in Children Jul 08, 2014 ACPE, IACET Online Instruction Global Online
    Advanced Clinical Statistics for Nonstatisticians Jul 15, 2014 ACPE, IACET Online Instruction Global Online
    Adverse Event Reporting Requirements: IND and Postmarketing Jul 22, 2014 IACET Online Instruction Global Online
    Planning and Managing Your Projects Jul 29, 2014 IACET, PMI Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 5: Technical Development: Pediatric Formulations Aug 12, 2014 ACPE, IACET Online Instruction Global Online
    Team Building and Development Aug 13, 2014 IACET, PMI Online Instruction Global Online
    Pragmatic Approaches to Drug Safety Across the Premarketing and Postmarketing Continuum Aug 18, 2014 ACPE, IACET In-Person Instruction North America
    Regulatory Affairs: The IND, NDA, and Postmarketing Aug 18, 2014 IACET In-Person Instruction North America Boston, MA, United States
    Clinical Project Management Aug 18, 2014 IACET, PMI In-Person Instruction North America Boston, MA, United States
    New Drug Product Development and Life Cycle Management Aug 18, 2014 IACET, PMI In-Person Instruction North America Boston, MA, United States
    European Regulatory Affairs: Keeping Your Finger on the Pulse of Marketing Authorizations Aug 18, 2014 IACET In-Person Instruction North America Boston, MA, United States
    Project Risk Management Aug 20, 2014 IACET, PMI In-Person Instruction North America Boston, MA, United States
    Overview of Drug Development Sep 08, 2014 IACET, PMI In-Person Instruction North America Horsham, PA, United States
    Key Considerations for the Development and Marketing of Biosimilar Products Sep 09, 2014 IACET In-Person Instruction North America Horsham, PA, United States
    Seven-Part Series on Pediatric Drug Development - Part 6: Preclinical Toxicology & Safety Sep 09, 2014 ACPE, IACET Online Instruction Global Online
    Art of Writing a Clinical Overview Sep 09, 2014 IACET Online Instruction Global Online
    Development of a Clinical Study Report Sep 15, 2014 IACET In-Person Instruction North America Rockville, MD, United States
    Clinical Statistics for Nonstatisticians Sep 15, 2014 ACPE, IACET In-Person Instruction North America Rockville, MD, United States
    EDM and ERS 2014 Sep 22, 2014 Meetings North America
    Strategies for Good Clinical Practice Audits Sep 23, 2014 IACET, RN Online Instruction Global Online
    Introduction to Signal Detection and Data Mining Sep 29, 2014 IACET Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 7: 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
    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
    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
    Pediatric Research Conference 2014: Transforming the Pediatric Research Landscape through Innovation and Forward Thinking Nov 06, 2014 Meetings North America
    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