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    Name Start Date Credits Format Region Location
    ISBS-DIA Joint Symposium on Biopharmaceutical Statistics Jun 27, 2015 Meetings China Beijing, China
    Clinical Investigator: Module 2 - Conducting the Study Jul 1, 2015 ACPE, CME Online Instruction North America Online
    Clinical Investigator: Module 1 - Study Preparation and Initiation Jul 1, 2015 ACPE, CME Online Instruction North America Online
    Informed Consent Jul 1, 2015 ACPE Online Instruction North America Online
    Crisis Management Jul 1, 2015 ACPE, IACET Online Instruction North America Online
    Database Management Jul 1, 2015 ACPE, IACET Online Instruction North America Online
    Literature Evaluation Jul 1, 2015 ACPE, IACET Online Instruction North America Online
    Literature Searching Jul 1, 2015 ACPE, IACET Online Instruction North America Online
    Medical Inquiries Jul 1, 2015 ACPE, IACET Online Instruction North America Online
    Medical Writing Jul 1, 2015 IACET Online Instruction North America Online
    Product Labeling Jul 1, 2015 ACPE, IACET Online Instruction North America Online
    Regulatory Issues Jul 1, 2015 ACPE, IACET Online Instruction North America Online
    Statistics for Medical Communications Professionals Jul 1, 2015 ACPE, IACET Online Instruction North America Online
    Expert Reactor Panel: IOM Report on Sharing Clinical Trial Data Jul 1, 2015 Online Instruction Global Online
    Novel Data Sources: The Positive Impact of Social Media and Online Networks for Engaging with Patients Jul 1, 2015 Online Instruction Global Online
    FDA’s Evolving Position on the Brief Summary and Adequate Directions for Use Guidance Jul 1, 2015 Online Instruction Global Online
    Target Product Profile – Strategies to Optimize Drug Development, Product Labeling, and Commercialization Jul 1, 2015 Online Instruction Global Online
    GVP Module IX Compliant Signal Management Systems in Pharmacovigilance: A Tale of Two Experiences Jul 1, 2015 Online Instruction Global Online
    Complimentary Webinar - Using Revolutionary Machine Learning to Find the Most Relevant Content to Drive Informed Decisions in Regulatory Intelligence Jul 1, 2015 Online Instruction Global Online
    The Role of the Clinical Data Manager Jul 1, 2015 Online Instruction Global Online
    Complimentary: Regulatory and Real World Evidence Challenges of Rare Diseases and Orphan Drugs Jul 1, 2015 Online Instruction Global Online
    FDA’s Role in Advancing the Science of Pharmacovigilance: Tools, Methods, and Pilot Programs Under Evaluation for the Analysis of Safety Signals Jul 1, 2015 Online Instruction Global Online
    Proarrhythmia Jul 1, 2015 Online Instruction Global Online
    Facets of Drug-Induced Kidney Injury and Regulatory Perspective Jul 1, 2015 Online Instruction Global Online
    Impact on Drug Development of Novel Translational Safety Biomarkers for Improved Detection of Drug-Induced Acute Kidney Injury Jul 1, 2015 Online Instruction Global Online
    A New Era of Open Dialog and Communication: The Impact of FDASIA, PDUFA V, and Critical Path Innovation Meetings Jul 1, 2015 Online Instruction Global Online
    Pharmacovigilance and Risk Management: Patient Perspective Jul 1, 2015 Online Instruction Global Online
    Drug Safety Regulatory Requirements Jul 1, 2015 ACPE, IACET Online Instruction Global Online
    Premarketing Clinical Trial Safety Jul 1, 2015 ACPE, IACET Online Instruction Global Online
    Postmarketing Safety Management Jul 1, 2015 ACPE, IACET Online Instruction Global Online
    Basics of Signal Detection and Pharmacoepidemiology Jul 1, 2015 ACPE, IACET Online Instruction Global Online
    Safety Audits and Inspections Jul 1, 2015 ACPE, IACET Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 1: Fundamentals of Clinical Pharmacology: Pharmacokinetics Jul 1, 2015 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 2: Fundamentals of Clinical Pharmacology: Pharmacodynamics Jul 1, 2015 Online Instruction Global Online
    Pharmacovigilance and Global Harmonization Updates Jul 1, 2015 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology For Drug Development - Part 3: Principles of Modeling and Simulation Jul 1, 2015 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 4: Determining the Safe First Human Dose Jul 1, 2015 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 5: Assessment of QT Prolongation Jul 1, 2015 Online Instruction Global Online
    Negotiation and Influence Jul 1, 2015 Online Instruction Global Online
    Introduction to Drug Safety Jul 1, 2015 ACPE, IACET Online Instruction Global Online
    How to Prepare for a Safety Inspection Jul 1, 2015 Online Instruction Global Online
    Implementation and Status of Periodic Benefit-Risk Evaluation Reporting (PBRER) in Canada Jul 1, 2015 Online Instruction Global Online
    Clinical Statistics for Nonstatisticians Jul 1, 2015 Online Instruction Global Online
    Advanced Clinical Statistics for Nonstatisticians Jul 1, 2015 Online Instruction Global Online
    Development of a Clinical Study Report Jul 1, 2015 Online Instruction Global Online
    Oversight of Clinical Monitoring: Trends and Strategies Jul 1, 2015 Online Instruction Global Online
    Art of Writing a Clinical Overview Jul 1, 2015 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 6: Preclinical Toxicology & Safety Jul 1, 2015 Online Instruction Global Online
    Complimentary - Need to Reinvent the Clinical Trial? Innovate, Collaborate & Integrate Jul 1, 2015 Online Instruction Global Online
    Complimentary Webinar - How to Cut Clinical Trial Timelines in Half Jul 1, 2015 Online Instruction Global Online
    Disruptive Innovation in Medical Information Jul 1, 2015 Online Instruction Global Online
    A Tour of FDA Jul 1, 2015 Online Instruction Global Online
    A Tour of Health Canada Jul 1, 2015 Online Instruction Global Online
    A Tour of Health Europe Jul 1, 2015 Online Instruction Global Online
    Aspects of Regulatory History Jul 1, 2015 Online Instruction Global Online
    Bioresearch Monitoring Program (BIMO): Introduction Jul 1, 2015 Online Instruction Global Online
    The Clinical Development Process: Investigational Product, Plan, and Data Management Jul 1, 2015 Online Instruction Global Online
    Ethical Review Boards Jul 1, 2015 Online Instruction Global Online
    Ethics as the Foundation to Clinical Research Jul 1, 2015 Online Instruction Global Online
    Awareness of FDA Inspections for Pharmaceutical Manufacturers Jul 1, 2015 Online Instruction Global Online
    Biotechnology: An Overview of Compliance Considerations Jul 1, 2015 Online Instruction Global Online
    Change Control Jul 1, 2015 Online Instruction Global Online
    Clinical Trial Audits and Consequences of Non-Compliance Jul 1, 2015 Online Instruction Global Online
    Computerized Systems Inspections in the Medical Device Industry Jul 1, 2015 Online Instruction Global Online
    European Union Clinical Trials Directive Jul 1, 2015 Online Instruction Global Online
    GMP Principals of SOPs Jul 1, 2015 Online Instruction Global Online
    GMP Updates - Enforcement Changes at the New FDA Jul 1, 2015 Online Instruction Global Online
    GMPs for API Bulk Manufacturers Jul 1, 2015 Online Instruction Global Online
    Good Clinical Practices (GCPs) for New Product Investigations Jul 1, 2015 Online Instruction Global Online
    Good Laboratory Practices (GLPs) Jul 1, 2015 Online Instruction Global Online
    GxPs Jul 1, 2015 Online Instruction Global Online
    HIPAA - The Impact on Clinical Research Jul 1, 2015 Online Instruction Global Online
    Introduction to GMPs Jul 1, 2015 Online Instruction Global Online
    Investigational Product Development Jul 1, 2015 Online Instruction Global Online
    ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials Jul 1, 2015 Online Instruction Global Online
    Key Concepts of Process Validation Jul 1, 2015 Online Instruction Global Online
    Laboratory Specimens for Clinical Research Jul 1, 2015 Online Instruction Global Online
    Medical Device Safety Reporting Jul 1, 2015 Online Instruction Global Online
    Orientation to GMP Compliance Jul 1, 2015 Online Instruction Global Online
    Overview of the Clinical Research Process Jul 1, 2015 Online Instruction Global Online
    Part 11: Electronic Records and Signatures - Application Jul 1, 2015 Online Instruction Global Online
    Part 11: Electronic Records; Electronic Signatures Jul 1, 2015 Online Instruction Global Online
    Principles of Good Documentation Jul 1, 2015 Online Instruction Global Online
    Protection of Human Subjects in Clinical Trials Jul 1, 2015 Online Instruction Global Online
    Selecting and Managing Clinical Contract Research Organizations (CROs) Jul 1, 2015 Online Instruction Global Online
    Understanding Post-Approval Changes Jul 1, 2015 Online Instruction Global Online
    Computerized Systems Inspections in the Pharmaceutical Industry Jul 1, 2015 Online Instruction Global Online
    Basics of the PhRMA Code Jul 1, 2015 Online Instruction Global Online
    Basics of AdvaMed Code Jul 1, 2015 Online Instruction Global Online
    Eucomed Guidelines on Interactions with Healthcare Professionals Jul 1, 2015 Online Instruction Global Online
    Introduction to Medical Device Health Care Compliance Jul 1, 2015 Online Instruction Global Online
    Foreign Corrupt Practices Act Jul 1, 2015 Online Instruction Global Online
    Global Anti-bribery Jul 1, 2015 Online Instruction Global Online
    Variations to Marketing Authorisation in Europe Jul 1, 2015 Online Instruction Global Online
    Registration of Monoclonal Antibodies Jul 1, 2015 Online Instruction Global Online
    How to Gain Approval to Market a Generic Medicinal Product in the USA Jul 1, 2015 Online Instruction Global Online
    Pharmacokinetics and Pharmacodynamics in Drug Registration Jul 1, 2015 Online Instruction Global Online
    Implementing Risk-Based Monitoring: Practical Approaches Jul 1, 2015 Online Instruction Global Online
    Complimentary - Innovative Strategies for Developing Safer Cancer Therapies Jul 1, 2015 Online Instruction Global Online
    eRegulatory and Intelligence Virtual Conference Archive Jul 1, 2015 Online Instruction Global Online
    Complimentary Archive Webinar - Next Generation Feasibility: Better Planning Through Simulation Jul 1, 2015 Online Instruction Global Online
    Planning and Managing Your Projects Jul 1, 2015 Online Instruction Global Online
    Team Building and Development Jul 1, 2015 Online Instruction Global Online
    Preparing a Clinical Trial Budget Jul 1, 2015 Online Instruction Global Online
    Overview of Drug Development Jul 1, 2015 IACET, PMI Online Instruction Global Online
    Discovery and Preclinical Testing Phases Jul 1, 2015 Online Instruction Global Online
    Phase 1 Studies Jul 1, 2015 Online Instruction Global Online
    Phase 2 Studies Jul 1, 2015 Online Instruction Global Online
    Phase 3 Studies and Regulatory Review Jul 1, 2015 Online Instruction Global Online
    Phase 4 and Life Cycle Management Jul 1, 2015 Online Instruction Global Online
    Postmarketing Requirements: The Legal Framework, How They Are Issued, Sponsor Obligations, and Challenges to Overcome Jul 1, 2015 Online Instruction Global Online
    Introduction to the European Union Institutions and Regulatory Authority Jul 1, 2015 Online Instruction Global Online
    Introduction to US Institutions and Regulatory Authority (FDA) Jul 1, 2015 Online Instruction Global Online
    Introduction to Japanese Institutions and Regulatory Authorities Jul 1, 2015 Online Instruction Global Online
    Overview of the CTD and eCTD Jul 1, 2015 Online Instruction Global Online
    Introduction to the International Conference on Harmonisation (ICH) Jul 1, 2015 Online Instruction Global Online
    The Regulatory Development of a Drug Jul 1, 2015 Online Instruction Global Online
    Basics of Clinical Trials Jul 1, 2015 Online Instruction Global Online
    How to Register Medicinal Products through the Centralized Procedure Jul 1, 2015 Online Instruction Global Online
    How to Register Medicinal Products through the Mutual Recognition Procedure Jul 1, 2015 Online Instruction Global Online
    How to Maintain Marketing Approvals in Europe for Centrally Authorised Products Jul 1, 2015 Online Instruction Global Online
    How to Register a New Drug in the USA Jul 1, 2015 Online Instruction Global Online
    How to Register Medicinal Products through the Decentralized Procedure Jul 1, 2015 Online Instruction Global Online
    Access to Unapproved Drugs through Compassionate Use Jul 1, 2015 Online Instruction Global Online
    Regulatory Requirements for the Conduct of Clinical Trials in Europe Jul 1, 2015 Online Instruction Global Online
    Orphan Drugs in the USA, European Union, and Japan Jul 1, 2015 Online Instruction Global Online
    Regulatory Requirements for the Submission of Investigational New Drug Applications in the USA (INDs) Jul 1, 2015 Online Instruction Global Online
    Meeting Opportunities with Regulatory Agencies Jul 1, 2015 Online Instruction Global Online
    Complementary - How New Electronic Trial Master File (eTMF) Data Standards Can Enhance Clinical Trial Efficiency and Quality Jul 1, 2015 Online Instruction Global Online
    Complimentary - Regulatory Solutions in the Cloud - 10 Questions You Can't Afford NOT to Ask Jul 1, 2015 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 Jul 1, 2015 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 2-Connecting the Research Community: Data Sharing–Perspectives from Academia and Patient Advocacy Groups Jul 1, 2015 Online Instruction Global Online
    Complimentary - From the Clinic to the CFO: Adaptive Trials and Financial Decision-Making Jul 1, 2015 Online Instruction Global Online
    Complimentary - The Affiliate Challenge – How to Improve Compliance and Efficiency when Working with Regional Affiliates Jul 1, 2015 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 1: Overall Challenge: The Vision of Better Medicines for Children Jul 1, 2015 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 3: Regulatory Framework EU Jul 1, 2015 Online Instruction Global Online
    Seven-Part Pediatric Drug Development Webinar Series - Part 4: Dosing in Children Jul 1, 2015 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 2: Regulatory Framework US Overview Jul 1, 2015 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 5: Technical Development: Pediatric Formulations Jul 1, 2015 Online Instruction Global Online
    Basics of the NDA Phase Jul 1, 2015 Online Instruction Global Online
    Regulatory Aspects of Prescription Drug/Biologics Advertising and Promotional Labeling Jul 1, 2015 Online Instruction Global Online
    Basics of the IND Phase Jul 1, 2015 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 7: Operational Challenges of Pediatric Clinical Trials Jul 1, 2015 Online Instruction Global Online
    Clinical Trials Transparency 3 Part Webinar Series - Part 3: Understanding the Legislation Landscape: Regulatory Updates from the FDA, EMA and Health Canada Jul 1, 2015 Online Instruction Global Online
    4th DIA CMC Forum in Japan Jul 2, 2015 Meetings Japan Tokyo, Japan
    Adverse Event Reporting Requirements: IND and Post-marketing Jul 13, 2015 IACET Online Instruction Global Online
    Interactions with the FDA during IND/NDA Phases Jul 16, 2015 IACET Online Instruction Global Online
    Global Regulatory Strategy and Drug Development in Asia-Pacific, Latin America, and Other Emerging Markets Aug 3, 2015 In-Person Instruction North America Washington, DC, United States
    Development of a Clinical Study Report Aug 10, 2015 IACET In-Person Instruction North America Boston, MA, United States
    Regulatory Affairs: The IND, NDA, and Postmarketing Aug 10, 2015 IACET In-Person Instruction North America Boston, MA, United States
    Pragmatic Approaches to Drug Safety Across the Premarketing and Postmarketing Continuum Aug 10, 2015 ACPE, IACET In-Person Instruction North America Boston, MA, United States
    European Regulatory Affairs: Keeping Your Finger on the Pulse of Marketing Authorizations Aug 11, 2015 In-Person Instruction North America Boston, MA, United States
    Clinical Project Management Aug 24, 2015 IACET, PMI In-Person Instruction North America Washington, DC, United States
    New Drug Product Development and Life Cycle Management Aug 26, 2015 IACET, PMI In-Person Instruction North America Washington, DC, United States
    2nd DIA Project Management Training Course for Clinical Study Sites Aug 29, 2015 In-Person Instruction Japan Tokyo, Japan
    Overview of Drug Development in Japan Sep 2, 2015 Online Instruction Global Online
    DIA/FDA Oligonucleotide-Based Therapeutic Conference 2015 Sep 9, 2015 Meetings North America Washington, DC, United States
    Key Considerations for Biosimilar R&D Workshop Sep 14, 2015 Meetings China
    Part 1: FDA Initiatives to Meet the Medical Needs of Pregnant and Lactating Women through Improved Labeling of Medical Products Sep 15, 2015 Online Instruction Global Online
    Clinical Project Management Part I Sep 16, 2015 In-Person Instruction Europe London, United Kingdom
    Patient Engagement in Benefit-Risk Assessment throughout the Life Cycle of Medical Products Sep 17, 2015 Meetings North America North Bethesda, MD, United States
    Clinical Trial Disclosure & Data Transparency – The Expanding Global Environment Sep 17, 2015 Meetings North America Bethesda, MD, United States
    Paediatric Investigation Plans (PIP) Sep 17, 2015 In-Person Instruction Europe London, United Kingdom
    Post-Authorisation Safety Studies (PASS) Sep 21, 2015 In-Person Instruction Europe Berlin, Germany
    Adaptive Design in Clinical Trials: When and How to Apply Sep 21, 2015 IACET In-Person Instruction North America Washington, DC, United States
    Medical Devices: Regulation and lifecycle management Sep 21, 2015 In-Person Instruction Europe Vienna, Austria
    Quality by Design - Making next generation process efficiency a reality for Chemical and Biotech Product Development and Optimisation Sep 21, 2015 In-Person Instruction Europe Vienna, Austria
    The New Medical Device Regulation Information Day Sep 22, 2015 Meetings Europe Vienna, Austria
    Drug and Device Combination Products 2015: Navigating Regulation, Enhancing Collaboration, and Accelerating Development Sep 28, 2015 Meetings North America Bethesda, MD, United States
    Joint MHRA/DIA Excellence in Pharmacovigilance Sep 28, 2015 In-Person Instruction Europe London, United Kingdom
    Pragmatic Approaches to Drug Safety Across the Premarketing and Postmarketing Continuum Sep 28, 2015 ACPE, IACET In-Person Instruction North America Toronto, ON, Canada
    Clinical Statistics for Nonstatisticians Sep 28, 2015 ACPE, IACET In-Person Instruction North America Washington, DC, United States
    Companion Diagnostics Sep 30, 2015 Meetings North America Bethesda, MD, United States
    Central Audit Methods for Site Image Interpretation in Clinical Trials Oct 1, 2015 Meetings North America North Bethesda, MD, United States
    Annual joint DIA/EFGCP/EMA Better Medicines for Children Conference Oct 1, 2015 Meetings Europe London, United Kingdom
    Study Endpoints Oct 5, 2015 Meetings North America Bethesda, MD, United States
    Introduction to Signal Detection and Data Mining Oct 5, 2015 IACET Online Instruction Global Online
    Achieving Meaningful Regulatory and Clinical Outcomes for Patients: Strategies in Rare Disease Therapy Development Oct 7, 2015 Meetings North America Bethesda, MD, United States
    4th DIA Statistics Workshop in Japan for Non-Statisticians Oct 8, 2015 Meetings Japan Tokyo, Japan
    The 1st DIA China Drug Discovery Innovation Conference & Exhibition Oct 11, 2015 Meetings China Shanghai, China
    Introduction to the role of QPPVs Oct 12, 2015 In-Person Instruction Europe London, United Kingdom
    9th European Forum for Qualified Person for Pharmacovigilance (QPPV) and Pre-Conference Workshop Oct 13, 2015 Meetings Europe London, United Kingdom
    3rd DIA Advanced Regulatory Affairs Training Course in Japan Oct 13, 2015 In-Person Instruction Japan Tokyo, Japan
    Part 2: Overcoming the Challenges of Conducting Postmarketing Studies in Pregnant and Lactating Women Oct 13, 2015 Online Instruction Global Online
    Practical GCP Compliance Auditing of Trials and Systems Oct 14, 2015 In-Person Instruction Europe London, United Kingdom
    Clinical Statistics for Nonstatisticians Oct 14, 2015 ACPE, IACET In-Person Instruction North America Durham, NC, United States
    How to manage a successful health authority interaction Oct 14, 2015 In-Person Instruction Europe London, United Kingdom
    Clinical Statistics for Non-Statisticians Oct 15, 2015 In-Person Instruction Europe London, United Kingdom
    Tutorial 1: Achieving Biosimilarity Through Matching of Critical Quality Attributes to Reference Product’s Oct 18, 2015 In-Person Instruction North America Bethesda, MD, United States
    Biosimilars 2015 Oct 19, 2015 Meetings North America Bethesda, MD, United States
    Clinical Trials Workshop - Are we ready for the implementation of the new Clinical Trial Regulation in 2016? Oct 26, 2015 Meetings Europe London, United Kingdom
    Risk Management and Safety Communication Oct 26, 2015 ACPE, IACET In-Person Instruction North America Washington, DC, United States
    DIA Annual Canadian Meeting 2015 Oct 27, 2015 Meetings North America Ottawa, ON, Canada
    Essentials of Clinical Study Management Nov 2, 2015 In-Person Instruction Europe Basel, Switzerland
    Benefit/Risk Management Nov 3, 2015 In-Person Instruction Europe Paris Montrouge, France
    Biosimilars Conference 2015 Nov 4, 2015 Meetings Europe London, United Kingdom
    Essentials and Overview of the Regulatory Framework in Europe Nov 4, 2015 In-Person Instruction Europe Paris Montrouge, France
    Signal Management in Pharmacovigilance Nov 5, 2015 In-Person Instruction Europe Paris Montrouge, France
    Postmarketing Drug Safety & Pharmacovigilance Nov 9, 2015 ACPE, IACET In-Person Instruction North America Philadelphia, PA, United States
    Building the eCTD - Practical solutions to compiling electronic submissions Nov 9, 2015 In-Person Instruction Europe Dubai, United Arab Emirates
    Regulatory Affairs: The IND, NDA, and Postmarketing Nov 9, 2015 IACET In-Person Instruction North America Philadelphia, PA, United States
    Navigating Chemistry, Manufacturing and Controls Through the Drug Development Process Nov 9, 2015 IACET In-Person Instruction North America Philadelphia, PA, United States
    9th Annual European Medical Information and Communications Conference Nov 10, 2015 Meetings Europe London, United Kingdom
    Part 3: Assessing the Safety of Medications and Vaccines in Pregnancy: The Vaccines and Medications in Pregnancy Surveillance System Nov 10, 2015 Online Instruction Global Online
    Advanced Clinical Statistics for NonStatisticians Nov 11, 2015 ACPE, IACET In-Person Instruction North America Philadelphia, PA, United States
    12th Annual Meeting DIA Japan 2015 Nov 15, 2015 Meetings Japan Tokyo, Japan
    US Regulatory Affairs: A Comprehensive Review of Regulatory Procedures for INDs and NDAs in the US Nov 16, 2015 In-Person Instruction Europe London, United Kingdom
    Clinical Project Management Part II Nov 16, 2015 In-Person Instruction Europe London, United Kingdom
    11th Middle East Regulatory Conference (MERC) 2015 Nov 17, 2015 Meetings Europe Riyadh, Saudi Arabia
    The Development of Biopharmaceuticals - The big picture, innovation and scientific requirements Nov 25, 2015 In-Person Instruction Europe Vienna, Austria
    Part 4: CDC’s Treating for Two Initiative and Other Federal Efforts to Disseminate Data for Informed Clinical Decision Making in Pregnancy and Lactation Dec 8, 2015 Online Instruction Global Online
    Pharmacovigilance and Risk Management Strategies 2016 Jan 25, 2016 Meetings North America
    19th Annual Workshop in Japan for Clinical Data Management Jan 28, 2016 Meetings Japan Tokyo, Japan
    Medical and Scientific Communications 2016 Annual Forum Mar 21, 2016 Meetings North America Kissimmee, FL, United States
    28th Annual EuroMeeting Apr 6, 2016 Meetings Europe Hamburg, Germany
    DIA/FDA Statistics 2016 Forum Apr 25, 2016 Meetings North America North Bethesda, MD, United States
    DIA 2016 52nd Annual Meeting Jun 26, 2016 Meetings North America Philadelphia, PA, United States