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    Name Start Date Credits Format Region Location
    EudraVigilance - electronic reporting of ICSRs in the EEA, 04-06 May 2015, San Marino May 4, 2015 In-Person Instruction Europe San Marino, San Marino
    Basics of the IND Phase May 4, 2015 IACET Online Instruction Global Online
    Oversight of Clinical Monitoring: Trends and Strategies May 5, 2015 IACET Online Instruction Global Online
    Clinical Investigator: Module 2 - Conducting the Study May 6, 2015 ACPE, CME Online Instruction North America Online
    Clinical Investigator: Module 1 - Study Preparation and Initiation May 6, 2015 ACPE, CME Online Instruction North America Online
    Informed Consent May 6, 2015 ACPE Online Instruction North America Online
    Crisis Management May 6, 2015 ACPE, IACET Online Instruction North America Online
    Database Management May 6, 2015 ACPE, IACET Online Instruction North America Online
    Literature Evaluation May 6, 2015 ACPE, IACET Online Instruction North America Online
    Literature Searching May 6, 2015 ACPE, IACET Online Instruction North America Online
    Medical Inquiries May 6, 2015 ACPE, IACET Online Instruction North America Online
    Medical Writing May 6, 2015 IACET Online Instruction North America Online
    Product Labeling May 6, 2015 ACPE, IACET Online Instruction North America Online
    Regulatory Issues May 6, 2015 ACPE, IACET Online Instruction North America Online
    Statistics for Medical Communications Professionals May 6, 2015 ACPE, IACET Online Instruction North America Online
    Expert Reactor Panel: IOM Report on Sharing Clinical Trial Data May 6, 2015 Online Instruction Global Online
    Novel Data Sources: The Positive Impact of Social Media and Online Networks for Engaging with Patients May 6, 2015 Online Instruction Global Online
    Generic Drug Labeling Proposed Rule and Safety Updates May 6, 2015 Online Instruction Global Online
    FDA’s Evolving Position on the Brief Summary and Adequate Directions for Use Guidance May 6, 2015 Online Instruction Global Online
    Target Product Profile – Strategies to Optimize Drug Development, Product Labeling, and Commercialization May 6, 2015 Online Instruction Global Online
    GVP Module IX Compliant Signal Management Systems in Pharmacovigilance: A Tale of Two Experiences May 6, 2015 Online Instruction Global Online
    Complimentary Webinar - Using Revolutionary Machine Learning to Find the Most Relevant Content to Drive Informed Decisions in Regulatory Intelligence May 6, 2015 Online Instruction Global Online
    The Role of the Clinical Data Manager May 6, 2015 Online Instruction Global Online
    Implementation of the FDASIA Patient Provisions May 6, 2015 Online Instruction Global Online
    Complimentary: Regulatory and Real World Evidence Challenges of Rare Diseases and Orphan Drugs May 6, 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 May 6, 2015 Online Instruction Global Online
    Variations in the European Union: CMC/Quality Changes May 6, 2015 Online Instruction Global Online
    Proarrhythmia May 6, 2015 Online Instruction Global Online
    Facets of Drug-Induced Kidney Injury and Regulatory Perspective May 6, 2015 Online Instruction Global Online
    Impact on Drug Development of Novel Translational Safety Biomarkers for Improved Detection of Drug-Induced Acute Kidney Injury May 6, 2015 Online Instruction Global Online
    Pharmacovigilance and Risk Management: Patient Perspective May 6, 2015 Online Instruction Global Online
    Drug Safety Regulatory Requirements May 6, 2015 ACPE, IACET Online Instruction Global Online
    Premarketing Clinical Trial Safety May 6, 2015 ACPE, IACET Online Instruction Global Online
    Postmarketing Safety Management May 6, 2015 ACPE, IACET Online Instruction Global Online
    Basics of Signal Detection and Pharmacoepidemiology May 6, 2015 ACPE, IACET Online Instruction Global Online
    Safety Audits and Inspections May 6, 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 May 6, 2015 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 2: Fundamentals of Clinical Pharmacology: Pharmacodynamics May 6, 2015 Online Instruction Global Online
    Pharmacovigilance and Global Harmonization Updates May 6, 2015 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology For Drug Development - Part 3: Principles of Modeling and Simulation May 6, 2015 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 4: Determining the Safe First Human Dose May 6, 2015 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 5: Assessment of QT Prolongation May 6, 2015 Online Instruction Global Online
    Negotiation and Influence May 6, 2015 Online Instruction Global Online
    Introduction to Drug Safety May 6, 2015 ACPE, IACET Online Instruction Global Online
    How to Prepare for a Safety Inspection May 6, 2015 Online Instruction Global Online
    Implementation and Status of Periodic Benefit-Risk Evaluation Reporting (PBRER) in Canada May 6, 2015 Online Instruction Global Online
    Clinical Statistics for Nonstatisticians May 6, 2015 Online Instruction Global Online
    Advanced Clinical Statistics for Nonstatisticians May 6, 2015 Online Instruction Global Online
    Development of a Clinical Study Report May 6, 2015 Online Instruction Global Online
    Art of Writing a Clinical Overview May 6, 2015 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 6: Preclinical Toxicology & Safety May 6, 2015 Online Instruction Global Online
    Complimentary - Need to Reinvent the Clinical Trial? Innovate, Collaborate & Integrate May 6, 2015 Online Instruction Global Online
    Complimentary Webinar - How to Cut Clinical Trial Timelines in Half May 6, 2015 Online Instruction Global Online
    Disruptive Innovation in Medical Information May 6, 2015 Online Instruction Global Online
    A Tour of FDA May 6, 2015 Online Instruction Global Online
    A Tour of Health Canada May 6, 2015 Online Instruction Global Online
    A Tour of Health Europe May 6, 2015 Online Instruction Global Online
    Aspects of Regulatory History May 6, 2015 Online Instruction Global Online
    Bioresearch Monitoring Program (BIMO): Introduction May 6, 2015 Online Instruction Global Online
    The Clinical Development Process: Investigational Product, Plan, and Data Management May 6, 2015 Online Instruction Global Online
    Ethical Review Boards May 6, 2015 Online Instruction Global Online
    Ethics as the Foundation to Clinical Research May 6, 2015 Online Instruction Global Online
    Awareness of FDA Inspections for Pharmaceutical Manufacturers May 6, 2015 Online Instruction Global Online
    Biotechnology: An Overview of Compliance Considerations May 6, 2015 Online Instruction Global Online
    Change Control May 6, 2015 Online Instruction Global Online
    Clinical Trial Audits and Consequences of Non-Compliance May 6, 2015 Online Instruction Global Online
    Computerized Systems Inspections in the Medical Device Industry May 6, 2015 Online Instruction Global Online
    European Union Clinical Trials Directive May 6, 2015 Online Instruction Global Online
    GMP Principals of SOPs May 6, 2015 Online Instruction Global Online
    GMP Updates - Enforcement Changes at the New FDA May 6, 2015 Online Instruction Global Online
    GMPs for API Bulk Manufacturers May 6, 2015 Online Instruction Global Online
    Good Clinical Practices (GCPs) for New Product Investigations May 6, 2015 Online Instruction Global Online
    Good Laboratory Practices (GLPs) May 6, 2015 Online Instruction Global Online
    GxPs May 6, 2015 Online Instruction Global Online
    HIPAA - The Impact on Clinical Research May 6, 2015 Online Instruction Global Online
    Introduction to GMPs May 6, 2015 Online Instruction Global Online
    Investigational Product Development May 6, 2015 Online Instruction Global Online
    ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials May 6, 2015 Online Instruction Global Online
    Key Concepts of Process Validation May 6, 2015 Online Instruction Global Online
    Laboratory Specimens for Clinical Research May 6, 2015 Online Instruction Global Online
    Medical Device Safety Reporting May 6, 2015 Online Instruction Global Online
    Orientation to GMP Compliance May 6, 2015 Online Instruction Global Online
    Overview of the Clinical Research Process May 6, 2015 Online Instruction Global Online
    Part 11: Electronic Records and Signatures - Application May 6, 2015 Online Instruction Global Online
    Part 11: Electronic Records; Electronic Signatures May 6, 2015 Online Instruction Global Online
    Principles of Good Documentation May 6, 2015 Online Instruction Global Online
    Protection of Human Subjects in Clinical Trials May 6, 2015 Online Instruction Global Online
    Selecting and Managing Clinical Contract Research Organizations (CROs) May 6, 2015 Online Instruction Global Online
    Understanding Post-Approval Changes May 6, 2015 Online Instruction Global Online
    Computerized Systems Inspections in the Pharmaceutical Industry May 6, 2015 Online Instruction Global Online
    Basics of the PhRMA Code May 6, 2015 Online Instruction Global Online
    Basics of AdvaMed Code May 6, 2015 Online Instruction Global Online
    Eucomed Guidelines on Interactions with Healthcare Professionals May 6, 2015 Online Instruction Global Online
    Introduction to Medical Device Health Care Compliance May 6, 2015 Online Instruction Global Online
    Foreign Corrupt Practices Act May 6, 2015 Online Instruction Global Online
    Global Anti-bribery May 6, 2015 Online Instruction Global Online
    Variations to Marketing Authorisation in Europe May 6, 2015 Online Instruction Global Online
    Registration of Monoclonal Antibodies May 6, 2015 Online Instruction Global Online
    How to Gain Approval to Market a Generic Medicinal Product in the USA May 6, 2015 Online Instruction Global Online
    Pharmacokinetics and Pharmacodynamics in Drug Registration May 6, 2015 Online Instruction Global Online
    Implementing Risk-Based Monitoring: Practical Approaches May 6, 2015 Online Instruction Global Online
    Complimentary - Innovative Strategies for Developing Safer Cancer Therapies May 6, 2015 Online Instruction Global Online
    Complimentary - Risk-Based Monitoring: Regulatory Expectation and Operational Application May 6, 2015 Online Instruction Global Online
    Fundamentals of Project Management for Nonproject Managers May 6, 2015 Online Instruction Global Online
    Planning and Managing Your Projects May 6, 2015 Online Instruction Global Online
    Team Building and Development May 6, 2015 Online Instruction Global Online
    Preparing a Clinical Trial Budget May 6, 2015 Online Instruction Global Online
    Postmarketing Requirements: The Legal Framework, How They Are Issued, Sponsor Obligations and Challenges to Overcome May 6, 2015 Online Instruction Global Online
    Introduction to the European Union Institutions and Regulatory Authority May 6, 2015 Online Instruction Global Online
    Introduction to US Institutions and Regulatory Authority (FDA) May 6, 2015 Online Instruction Global Online
    Introduction to Japanese Institutions and Regulatory Authorities May 6, 2015 Online Instruction Global Online
    Overview of the CTD and eCTD May 6, 2015 Online Instruction Global Online
    Introduction to the International Conference on Harmonisation (ICH) May 6, 2015 Online Instruction Global Online
    The Regulatory Development of a Drug May 6, 2015 Online Instruction Global Online
    Basics of Clinical Trials May 6, 2015 Online Instruction Global Online
    How to Register Medicinal Products through the Centralized Procedure May 6, 2015 Online Instruction Global Online
    How to Register Medicinal Products through the Mutual Recognition Procedure May 6, 2015 Online Instruction Global Online
    How to Maintain Marketing Approvals in Europe for Centrally Authorised Products May 6, 2015 Online Instruction Global Online
    How to Register a New Drug in the USA May 6, 2015 Online Instruction Global Online
    How to Register Medicinal Products through the Decentralized Procedure May 6, 2015 Online Instruction Global Online
    Access to Unapproved Drugs through Compassionate Use May 6, 2015 Online Instruction Global Online
    Regulatory Requirements for the Conduct of Clinical Trials in Europe May 6, 2015 Online Instruction Global Online
    Orphan Drugs in the USA, European Union, and Japan May 6, 2015 Online Instruction Global Online
    Regulatory Requirements for the Submission of Investigational New Drug Applications in the USA (INDs) May 6, 2015 Online Instruction Global Online
    Meeting Opportunities with Regulatory Agencies May 6, 2015 Online Instruction Global Online
    Complementary - How New Electronic Trial Master File (eTMF) Data Standards Can Enhance Clinical Trial Efficiency and Quality May 6, 2015 Online Instruction Global Online
    Complimentary - Regulatory Solutions in the Cloud - 10 Questions You Can't Afford NOT to Ask May 6, 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 May 6, 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 May 6, 2015 Online Instruction Global Online
    Complimentary - From the Clinic to the CFO: Adaptive Trials and Financial Decision-Making May 6, 2015 Online Instruction Global Online
    Adverse Event Reporting Requirements: IND and Postmarketing May 6, 2015 Online Instruction Global Online
    Complimentary - The Affiliate Challenge – How to Improve Compliance and Efficiency when Working with Regional Affiliates May 6, 2015 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 1: Overall Challenge: The Vision of Better Medicines for Children May 6, 2015 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 3: Regulatory Framework EU May 6, 2015 Online Instruction Global Online
    Seven-Part Pediatric Drug Development Webinar Series - Part 4: Dosing in Children May 6, 2015 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 2: Regulatory Framework US Overview May 6, 2015 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 5: Technical Development: Pediatric Formulations May 6, 2015 Online Instruction Global Online
    Regulatory Aspects of Prescription Drug/Biologics Advertising and Promotional Labeling May 6, 2015 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 7: Operational Challenges of Pediatric Clinical Trials May 6, 2015 Online Instruction Global Online
    Supplements and Other Changes to an Approved Application May 6, 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 May 6, 2015 Online Instruction Global Online
    Tutorial #1 – IDMP? What Is That and How Do I Get Started? May 11, 2015 IACET In-Person Instruction North America Philadelphia, PA, United States
    eRegulatory and Intelligence Annual Conference May 11, 2015 IACET Meetings North America Philadelphia, PA, United States
    eRegulatory and Intelligence Virtual Conference May 11, 2015 Meetings Global
    Complimentary Webinar - Next Generation Feasibility: Better Planning Through Simulation May 13, 2015 Online Instruction Global Online
    Electronic Submissions: The Next Era of Electronic Submissions May 14, 2015 IACET In-Person Instruction North America Philadelphia, PA, United States
    Pre-Marketing Clinical Safety May 18, 2015 In-Person Instruction Europe London, United Kingdom
    Oncology Drug-Induced Cardiotoxicity Conference May 18, 2015 Meetings Europe Basel, Switzerland
    5th DIA Project Management Training Course in Japan May 18, 2015 PMI In-Person Instruction Japan Kyoto, Japan
    Basics of the NDA Phase May 18, 2015 IACET Online Instruction Global Online
    Introduction to Pharmacovigilance and Rules for Expedited Reporting of Individual Case Safety Reports (ICSRs) in Europe May 19, 2015 In-Person Instruction Europe London, United Kingdom
    Postmarketing Requirements: The Legal Framework, How They Are Issued, Sponsor Obligations and Challenges to Overcome May 19, 2015 ACPE, IACET Online Instruction Global Online
    EudraVigilance - electronic reporting of ICSRs in the EEA May 20, 2015 In-Person Instruction Europe London, United Kingdom
    Tutorial 1: PBRERs May 20, 2015 IACET In-Person Instruction North America Toronto, ON, Canada
    DIA Canadian Pharmacovigilance & Risk Management Meeting May 21, 2015 IACET Meetings North America Toronto, ON, Canada
    1st DIA Risk Management & Safety Communication Strategies Training Course in Japan May 21, 2015 In-Person Instruction Japan Tokyo, Japan
    The 7th DIA China Annual Meeting May 24, 2015 Meetings China Shanghai, China
    How to Prepare for a Safety Inspection Jun 1, 2015 IACET Online Instruction Global Online
    EudraVigilance - electronic reporting of ICSRs in the EEA Jun 3, 2015 In-Person Instruction Europe Berlin, Germany
    2nd DIA European Medicines Regulations and the EU-Network Training Course Jun 4, 2015 In-Person Instruction Japan Tokyo, Japan
    FDA’s Role in Advancing the Science of Pharmacovigilance: Tools, Methods, and Pilot Programs Under Evaluation for the Analysis of Safety Signals Jun 4, 2015 Online Instruction Global Online
    Joint DIA/EMA Information Day on Post-Authorisation Studies (PAS) Jun 5, 2015 In-Person Instruction Europe London, United Kingdom
    EudraVigilance - electronic reporting of ICSRs in the EEA Jun 8, 2015 In-Person Instruction Europe London, United Kingdom
    Medical Approach in Diagnosis and Management of ADRs Jun 10, 2015 In-Person Instruction Europe Paris Montrouge, France
    eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) Jun 11, 2015 In-Person Instruction Europe London, United Kingdom
    Diagnosis and Management of Drug-Induced Liver Injury (DILI) Jun 11, 2015 In-Person Instruction Europe Paris Montrouge, France
    #20: The Sunshine Act: Understanding the Essentials of Compliance Jun 14, 2015 CME, IACET, RN In-Person Instruction North America Washington, DC, United States
    #21: Leadership: How to Organize and Lead People in a Work Group Jun 14, 2015 IACET, PMI In-Person Instruction North America Washington, DC, United States
    #22: Successful Drug Development: Best Practices for Clinical Trial Design, Agency Interactions, and Regulatory Document Writing Jun 14, 2015 IACET In-Person Instruction North America Washington, DC, United States
    #23: How to Prepare for an FDA Inspection Jun 14, 2015 CME, IACET, RN In-Person Instruction North America Washington, DC, United States
    #24: Pharmacogenomics and Companion Diagnostics: The Future of Clinical Trials, New Product Development and the Practice of Medicine Jun 14, 2015 ACPE, CME, IACET, RN In-Person Instruction North America Washington, DC, United States
    #25: Signal Detection: Identifying and Managing Safety Signals Jun 14, 2015 ACPE, CME, IACET, RN In-Person Instruction North America Washington, DC, United States
    DIA 2015 51st Annual Meeting: Develop. Innovate. Advance. Jun 14, 2015 ACPE, CME, IACET, RN, PMI Meetings North America Washington, DC, United States
    #40: Analysis of Safety Data from Clinical Trials Jun 14, 2015 ACPE, CME, IACET, RN In-Person Instruction North America Washington, DC, United States
    #41: Quality Oversight of CROs-Clinical Vendors Jun 14, 2015 IACET In-Person Instruction North America Washington, DC, United States
    #42: Fundamentals of ANDA Submissions and FDA Expectations Under GDUFA Jun 14, 2015 CME, IACET, RN In-Person Instruction North America Washington, DC, United States
    #43: Clinical Statistics for Nonstatisticians Jun 14, 2015 ACPE, CME, IACET, RN In-Person Instruction North America Washington, DC, United States
    #44: Risk Management and Safety Communication Strategies Jun 14, 2015 ACPE, CME, IACET, RN In-Person Instruction North America Washington, DC, United States
    #45: The Good Pharmacovigilance Practices in the EU: Global Applications Jun 14, 2015 CME, IACET, RN In-Person Instruction North America Washington, DC, United States
    #30: Japan Regulatory Environment: Overview of the Organization, Processes, Systems, and Changes Affecting Pharmaceutical Development Jun 14, 2015 IACET In-Person Instruction North America Washington, DC, United States
    #31: Preparing for a US FDA Advisory Committee Meeting Jun 14, 2015 IACET In-Person Instruction North America Washington, DC, United States
    #32: Influencing Culture, Avoiding Bureaucracy, and Encouraging Innovation Jun 14, 2015 IACET In-Person Instruction North America Washington, DC, United States
    #33: Large-Scale Regulatory Functional Outsourcing: Emerging Trends, Challenges, and Decision Criteria Jun 14, 2015 IACET In-Person Instruction North America Washington, DC, United States
    #34: Preparation of Risk Evaluation and Mitigation Strategies Assessment Reports Jun 14, 2015 ACPE, CME, IACET, RN In-Person Instruction North America Washington, DC, United States
    #35: Ethical Issues in Clinical Trials Jun 14, 2015 CME, IACET, RN In-Person Instruction North America Washington, DC, United States
    Joint EMA/DIA Information Day on ISO IDMP standards: Achieving Compliance Jun 23, 2015 In-Person Instruction Europe London, United Kingdom
    4th Global Animal Health Conference 2015: regulatory convergence Jun 24, 2015 Meetings Europe Dar Es Salaam, Tanzania, United Republic of
    ISBS-DIA Joint Symposium on Biopharmaceutical Statistics Jun 27, 2015 Meetings China Beijing, China
    Joint EMA/DIA Information Day on Risk Management Planning Jun 30, 2015 In-Person Instruction Europe London, United Kingdom
    DIA-TOPRA Workshop on Adaptive Pathways Jun 30, 2015 Meetings Europe Brussels, Belgium
    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 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
    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
    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
    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
    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
    Medical Devices: Regulation and lifecycle management Sep 21, 2015 In-Person Instruction Europe Vienna, Austria
    Quality by Design - New Concepts 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
    Annual joint DIA/EFGCP/EMA Better Medicines for Children Conference Oct 1, 2015 Meetings Europe London, United Kingdom
    Introduction to Signal Detection and Data Mining Oct 5, 2015 IACET Online Instruction Global Online
    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
    Practical GCP Compliance Auditing of Trials and Systems Oct 14, 2015 In-Person Instruction Europe London, United Kingdom
    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 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
    DIA Annual Canadian Meeting 2015 Call for Abstracts Oct 27, 2015 Meetings North America Ottawa, ON, Canada
    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 of European Regulatory Affairs 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
    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
    Biopharmaceuticals, Biosimilars and Advanced Therapies in Europe - Development and Regulatory Framework Nov 25, 2015 In-Person Instruction Europe Vienna, Austria