DIA
Drug Information Association Logo

Advanced Search

MM-DD-YYYY

Add Filter

    Advanced Search

    Find Meetings & Training 

    Name Start Date Credits Format Region Location
    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
    EudraVigilance - electronic reporting of ICSRs in the EEA Oct 20, 2014 In-Person Instruction Europe San Marino, San Marino
    Clinical Investigator: Module 2 - Conducting The Study Oct 20, 2014 ACPE, CME Online Instruction North America Online
    Clinical Investigator: Module 1 - Study Preparation and Initiation Oct 20, 2014 ACPE, CME Online Instruction North America Online
    Informed Consent Oct 20, 2014 ACPE Online Instruction North America Online
    Crisis Management Oct 20, 2014 ACPE, IACET Online Instruction North America Online
    Database Management Oct 20, 2014 ACPE, IACET Online Instruction North America Online
    Literature Evaluation Oct 20, 2014 ACPE, IACET Online Instruction North America Online
    Literature Searching Oct 20, 2014 ACPE, IACET Online Instruction North America Online
    Medical Inquiries Oct 20, 2014 ACPE, IACET Online Instruction North America Online
    Medical Writing Oct 20, 2014 IACET Online Instruction North America Online
    Product Labeling Oct 20, 2014 ACPE, IACET Online Instruction North America Online
    Regulatory Issues Oct 20, 2014 ACPE, IACET Online Instruction North America Online
    Statistics for Medical Communications Professionals Oct 20, 2014 ACPE, IACET Online Instruction North America Online
    The Use of Mobile Medical Applications as Companions Oct 20, 2014 Online Instruction Global Online
    Generic Drug Labeling Proposed Rule and Safety Updates Oct 20, 2014 Online Instruction Global Online
    Emerging Technologies to Rare Disorder Drug Development: Promises and Pitfalls Oct 20, 2014 Online Instruction Global Online
    Big Data: Impact of Health Care Reform on Collaborations and Strategies Oct 20, 2014 Online Instruction Global Online
    The Role of the Clinical Data Manager Oct 20, 2014 Online Instruction Global Online
    Implementation of the FDASIA Patient Provisions Oct 20, 2014 Online Instruction Global Online
    Complimentary: Regulatory and Real World Evidence Challenges of Rare Diseases and Orphan Drugs Oct 20, 2014 Online Instruction Global Online
    Variations in the European Union: CMC/Quality Changes Oct 20, 2014 Online Instruction Global Online
    Good Pharmacovigilance Practice: How Good has it Proven to be for Industry? Oct 20, 2014 Online Instruction Global Online
    Pharmacovigilance and Risk Management: Patient Perspective Oct 20, 2014 Online Instruction Global Online
    Complimentary Patient-Centeredness and Engagement in Clinical Research: Opportunities for Industry Oct 20, 2014 Online Instruction Global Online
    Drug Safety Regulatory Requirements Oct 20, 2014 ACPE, IACET Online Instruction Global Online
    Premarketing Clinical Trial Safety Oct 20, 2014 ACPE, IACET Online Instruction Global Online
    Postmarketing Safety Management Oct 20, 2014 ACPE, IACET Online Instruction Global Online
    Basics of Signal Detection and Pharmacoepidemiology Oct 20, 2014 ACPE, IACET Online Instruction Global Online
    Safety Audits and Inspections Oct 20, 2014 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 1: Fundamentals of Clinical Pharmacology: Pharmacokinetics Oct 20, 2014 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 2: Fundamentals of Clinical Pharmacology: Pharmacodynamics Oct 20, 2014 Online Instruction Global Online
    Pharmacovigilance and Global Harmonization Updates Oct 20, 2014 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology For Drug Development - Part 3: Principles of Modeling and Simulation Oct 20, 2014 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 4: Determining the Safe First Human Dose Oct 20, 2014 Online Instruction Global Online
    Designed for Success: Utilizing Protocol Quality by Design (QbD) to Plan Clinical Studies Oct 20, 2014 Online Instruction Global Online
    Negotiation and Influence Oct 20, 2014 Online Instruction Global Online
    China Update: Regulatory Changes and Implications Oct 20, 2014 Online Instruction Global Online
    Evaluation and Management of Cardiac Conditions in Oncology Patients Oct 20, 2014 Online Instruction Global Online
    Introduction to Drug Safety Oct 20, 2014 ACPE, IACET Online Instruction Global Online
    How to Prepare for a Safety Inspection Oct 20, 2014 Online Instruction Global Online
    Clinical Statistics for Nonstatisticians Oct 20, 2014 Online Instruction Global Online
    Advanced Clinical Statistics for Nonstatisticians Oct 20, 2014 Online Instruction Global Online
    Development of a Clinical Study Report Oct 20, 2014 Online Instruction Global Online
    Art of Writing a Clinical Overview Oct 20, 2014 Online Instruction Global Online
    CardioVascular Safety: The New Paradigm - Proarrhythmic Assessment of New Drugs without the Thorough QT Study Oct 20, 2014 Online Instruction Global Online
    CardioVascular Safety – What are the Key Issues Regarding Blood Pressure Assessment During Clinical Development Oct 20, 2014 Online Instruction Global Online
    Introductory Principles and Application of Risk Management within Clinical Operations Oct 20, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 6: Preclinical Toxicology & Safety Oct 20, 2014 Online Instruction Global Online
    Electronic Submissions 101 – Essential MS Word and Adobe Acrobat Tools/Skills and Current IT Options Oct 20, 2014 Online Instruction Global Online
    Disruptive Innovation in Medical Information Oct 20, 2014 Online Instruction Global Online
    A Tour of FDA Oct 20, 2014 Online Instruction Global Online
    A Tour of Health Canada Oct 20, 2014 Online Instruction Global Online
    A Tour of Health Europe Oct 20, 2014 Online Instruction Global Online
    Aspects of Regulatory History Oct 20, 2014 Online Instruction Global Online
    Bioresearch Monitoring Program (BIMO): Introduction Oct 20, 2014 Online Instruction Global Online
    The Clinical Development Process: Investigational Product, Plan, and Data Management Oct 20, 2014 Online Instruction Global Online
    Drug Safety & Adverse Event Reporting Oct 20, 2014 Online Instruction Global Online
    Ethical Review Boards Oct 20, 2014 Online Instruction Global Online
    Ethics as the Foundation to Clinical Research Oct 20, 2014 Online Instruction Global Online
    Awareness of FDA Inspections for Pharmaceutical Manufacturers Oct 20, 2014 Online Instruction Global Online
    Biotechnology: An Overview of Compliance Considerations Oct 20, 2014 Online Instruction Global Online
    Change Control Oct 20, 2014 Online Instruction Global Online
    Clinical Trial Audits and Consequences of Non-Compliance Oct 20, 2014 Online Instruction Global Online
    Computerized Systems Inspections in the Medical Device Industry Oct 20, 2014 Online Instruction Global Online
    European Union Clinical Trials Directive Oct 20, 2014 Online Instruction Global Online
    GMP Principals of SOPs Oct 20, 2014 Online Instruction Global Online
    GMP Updates - Enforcement Changes at the New FDA Oct 20, 2014 Online Instruction Global Online
    GMPs for API Bulk Manufacturers Oct 20, 2014 Online Instruction Global Online
    Good Clinical Practices (GCPs) for New Product Investigations Oct 20, 2014 Online Instruction Global Online
    Good Laboratory Practices (GLPs) Oct 20, 2014 Online Instruction Global Online
    GxPs Oct 20, 2014 Online Instruction Global Online
    HIPAA - The Impact on Clinical Research Oct 20, 2014 Online Instruction Global Online
    Introduction to GMPs Oct 20, 2014 Online Instruction Global Online
    Investigational Product Development Oct 20, 2014 Online Instruction Global Online
    ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials Oct 20, 2014 Online Instruction Global Online
    Key Concepts of Process Validation Oct 20, 2014 Online Instruction Global Online
    Laboratory Specimens for Clinical Research Oct 20, 2014 Online Instruction Global Online
    Medical Device Safety Reporting Oct 20, 2014 Online Instruction Global Online
    Orientation to GMP Compliance Oct 20, 2014 Online Instruction Global Online
    Overview of the Clinical Research Process Oct 20, 2014 Online Instruction Global Online
    Part 11: Electronic Records and Signatures - Application Oct 20, 2014 Online Instruction Global Online
    Part 11: Electronic Records; Electronic Signatures Oct 20, 2014 Online Instruction Global Online
    Principles of Good Documentation Oct 20, 2014 Online Instruction Global Online
    Protection of Human Subjects in Clinical Trials Oct 20, 2014 Online Instruction Global Online
    Selecting and Managing Clinical Contract Research Organizations (CROs) Oct 20, 2014 Online Instruction Global Online
    Understanding Post-Approval Changes Oct 20, 2014 Online Instruction Global Online
    Computerized Systems Inspections in the Pharmaceutical Industry Oct 20, 2014 Online Instruction Global Online
    Basics of the PhRMA Code Oct 20, 2014 Online Instruction Global Online
    Basics of AdvaMed Code Oct 20, 2014 Online Instruction Global Online
    Eucomed Guidelines on Interactions with Healthcare Professionals Oct 20, 2014 Online Instruction Global Online
    Introduction to Medical Device Health Care Compliance Oct 20, 2014 Online Instruction Global Online
    Foreign Corrupt Practices Act Oct 20, 2014 Online Instruction Global Online
    Global Anti-bribery Oct 20, 2014 Online Instruction Global Online
    Variations to Marketing Authorisation in Europe Oct 20, 2014 Online Instruction Global Online
    Registration of Monoclonal Antibodies Oct 20, 2014 Online Instruction Global Online
    How to Gain Approval to Market a Generic Medicinal Product in the USA Oct 20, 2014 Online Instruction Global Online
    Pharmacokinetics and Pharmacodynamics in Drug Registration Oct 20, 2014 Online Instruction Global Online
    Complimentary - Planning and Implementing Large Cardiovascular Outcomes Studies: Opportunities & Challenges Oct 20, 2014 Online Instruction Global Online
    Complimentary - Press the Easy Button – Ensure Consistency and Compliance for your Documents through Automation Oct 20, 2014 Online Instruction Global Online
    Complimentary - When Outsourcing Stops Making Sense Oct 20, 2014 Online Instruction Global Online
    Complimentary Quintiles/DIA Webinar - Giving Your Study The Right Start Toward Success Through Optimal Country and Site Selection Oct 20, 2014 Online Instruction Global Online
    Complimentary - Risk-Based Monitoring: Regulatory Expectation and Operational Application Oct 20, 2014 Online Instruction Global Online
    Fundamentals of Project Management for Nonproject Managers Oct 20, 2014 Online Instruction Global Online
    Planning and Managing Your Projects Oct 20, 2014 Online Instruction Global Online
    Project Risk Management: Dealing with the Certainty of Uncertainty Oct 20, 2014 Online Instruction Global Online
    Team Building and Development Oct 20, 2014 Online Instruction Global Online
    Preparing a Clinical Trial Budget Oct 20, 2014 Online Instruction Global Online
    Team Building and Development Oct 20, 2014 Online Instruction Global Online
    Introduction to the European Union Institutions and Regulatory Authority Oct 20, 2014 Online Instruction Global Online
    Introduction to US Institutions and Regulatory Authority (FDA) Oct 20, 2014 Online Instruction Global Online
    Introduction to Japanese Institutions and Regulatory Authorities Oct 20, 2014 Online Instruction Global Online
    Overview of the CTD and eCTD Oct 20, 2014 Online Instruction Global Online
    Introduction to the International Conference on Harmonisation (ICH) Oct 20, 2014 Online Instruction Global Online
    The Regulatory Development of a Drug Oct 20, 2014 Online Instruction Global Online
    Basics of Clinical Trials Oct 20, 2014 Online Instruction Global Online
    How to Register Medicinal Products through the Centralized Procedure Oct 20, 2014 Online Instruction Global Online
    How to Register Medicinal Products through the Mutual Recognition Procedure Oct 20, 2014 Online Instruction Global Online
    How to Maintain Marketing Approvals in Europe for Centrally Authorised Products Oct 20, 2014 Online Instruction Global Online
    How to Register a New Drug in the USA Oct 20, 2014 Online Instruction Global Online
    How to Register Medicinal Products through the Decentralized Procedure Oct 20, 2014 Online Instruction Global Online
    Access to Unapproved Drugs through Compassionate Use Oct 20, 2014 Online Instruction Global Online
    Regulatory Requirements for the Conduct of Clinical Trials in Europe Oct 20, 2014 Online Instruction Global Online
    Orphan Drugs in the USA, European Union, and Japan Oct 20, 2014 Online Instruction Global Online
    Regulatory Requirements for the Submission of Investigational New Drug Applications in the USA (INDs) Oct 20, 2014 Online Instruction Global Online
    Meeting Opportunities with Regulatory Agencies Oct 20, 2014 Online Instruction Global Online
    Combination Products and Convergence: An Overview of Clinical Benefits, Regulatory Issues & Manufacturing Challenges Oct 20, 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 Oct 20, 2014 Online Instruction Global Online
    Strategies for Successfully Introducing REMS to Your Organization: From Development and Implementation and Internal and External Evaluation Oct 20, 2014 Online Instruction Global Online
    The Case of the New England Compounding Center: Learning from the Tragedy Oct 20, 2014 Online Instruction Global Online
    Complimentary - From the Clinic to the CFO: Adaptive Trials and Financial Decision-Making Oct 20, 2014 Online Instruction Global Online
    Adverse Event Reporting Requirements: IND and Postmarketing Oct 20, 2014 Online Instruction Global Online
    Complimentary - The Affiliate Challenge – How to Improve Compliance and Efficiency when Working with Regional Affiliates Oct 20, 2014 Online Instruction Global Online
    The Future of Personalized Medicine and Companion Diagnostics Oct 20, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 1: Overall Challenge: The Vision of Better Medicines for Children Oct 20, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 3: Regulatory Framework EU Oct 20, 2014 Online Instruction Global Online
    Seven-Part Pediatric Drug Development Webinar Series - Part 4: Dosing in Children Oct 20, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 2: Regulatory Framework US Overview Oct 20, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 5: Technical Development: Pediatric Formulations Oct 20, 2014 Online Instruction Global Online
    Basics of the IND Oct 20, 2014 Online Instruction Global Online
    Basics of the NDA Oct 20, 2014 Online Instruction Global Online
    Regulatory Aspects of Prescription Drug/Biologics Advertising and Promotional Labeling Oct 20, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 7: Operational Challenges of Pediatric Clinical Trials Oct 20, 2014 Online Instruction Global Online
    Supplements and Other Changes to an Approved Application Oct 20, 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 2-Connecting the Research Community: Data Sharing–Perspectives from Academia and Patient Advocacy Groups Oct 21, 2014 IACET Online Instruction Global Online
    Practical GCP Compliance Auditing of Trials and Systems Oct 22, 2014 In-Person Instruction Europe London, United Kingdom
    Biopharmaceuticals, Biosimilars and Advanced Therapies - Development and Regulatory Framework in Europe Oct 22, 2014 In-Person Instruction Europe London, United Kingdom
    Complimentary - Regulatory Solutions in the Cloud – 10 Questions You Can’t Afford NOT to Ask Oct 22, 2014 Online Instruction Global Online
    Clinical Statistics for Non-Statisticians Oct 23, 2014 In-Person Instruction Europe London, United Kingdom
    5th DIA Cardiac Safety Workshop in Japan Oct 23, 2014 Meetings Japan Tokyo, Japan
    4th DIA Project Management Training Course in Japan Oct 27, 2014 PMI In-Person Instruction Japan Tokyo, Japan
    Non-Inferiority Trials – Design and Analysis Issues 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 ACPE, IACET 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
    How New Electronic Trial Master File (eTMF) Data Standards Can Enhance Clinical Trial Efficiency and Quality Oct 28, 2014 Online Instruction Global Online
    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
    Competing Regulatory Oversight of Investigational Tests, including LDTs, for Co-Development Programs Oct 29, 2014 In-Person Instruction 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
    Quantitative Science Forum Oct 31, 2014 Meetings China Beijing, China
    Multicentre International Data Integrity Workshop (Mumbai) Nov 03, 2014 In-Person Instruction India Andheri East, MH, India
    Navigating Chemistry, Manufacturing & Controls Through the Drug Development Process Nov 03, 2014 IACET In-Person Instruction North America Horsham, PA, United States
    How to Prepare for Pharmacovigilance Audits and Inspections Nov 03, 2014 In-Person Instruction Europe Charenton Le Pont, Paris, France
    Advanced Signal Detection - Tools, Triage, Evaluation, and Escalation Nov 03, 2014 IACET In-Person Instruction North America Washington, DC, United States
    Essentials of European Regulatory Affairs Nov 03, 2014 In-Person Instruction Europe Charenton Le Pont, Paris, France
    Signal Management in Pharmacovigilance Nov 03, 2014 In-Person Instruction Europe Charenton Le Pont, Paris, France
    Essentials of Clinical Study Management Nov 05, 2014 In-Person Instruction Europe London, United Kingdom
    US Regulatory Affairs Nov 05, 2014 In-Person Instruction Europe London, United Kingdom
    Multicentre International Data Integrity Workshop (Mumbai) Nov 06, 2014 In-Person Instruction India Andheri East, MH, India
    ISPE/DIA Workshop on Computer Systems Compliance “Maintain Data Integrity to Reduce Risk for the Patient” Nov 06, 2014 Meetings Europe Basel, Switzerland
    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
    Multicentre International Data Integrity Workshop (Hyderabad) Nov 10, 2014 In-Person Instruction India Hyderabad, India
    Benefit/Risk Management Nov 10, 2014 In-Person Instruction Europe Barcelona, Spain
    Clinical Project Management Part II Nov 10, 2014 In-Person Instruction Europe Barcelona, Spain
    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
    Joint DIA/AEMPS Statistics Workshop Nov 10, 2014 Meetings Europe Barcelona, Spain
    EudraVigilance - electronic reporting of ICSRs in the EEA Nov 10, 2014 In-Person Instruction Europe Vienna, Austria
    Tutorial: AN INTRODUCTION TO THE JOINT MODELLING OF LONGITUDINAL AND SURVIVAL DATA Nov 10, 2014 In-Person Instruction Europe Barcelona, Spain
    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
    Multicentre International Data Integrity Workshop (Bangalore) Nov 13, 2014 In-Person Instruction India Bangalore, India
    11th Annual Meeting DIA Japan 2014 Nov 16, 2014 Meetings Japan Tokyo, Japan
    #1 Basic Introduction for Non-Specialist: Drug-Drug Interaction and Summary of Change in New Japanese Drug-Drug Interaction Guideline Nov 16, 2014 In-Person Instruction Japan Tokyo, Japan
    #2 Next Steps for Content of Company Core Data Sheet Prepared by Western Companies - Part 1 Nov 16, 2014 In-Person Instruction Japan Tokyo, Japan
    #3 Action Learning for Six Sigma Analytical Tools Using Real Case Studies Nov 16, 2014 In-Person Instruction Japan Tokyo, Japan
    #4 Coaching as a Diverse Communication Tool Across Functions and Areas Nov 16, 2014 In-Person Instruction Japan Tokyo, Japan
    #5 The Basics of “Investigator Initiated Trial (IIT)” Regulation Nov 16, 2014 In-Person Instruction Japan Tokyo, Japan
    #6 Prediction for Human Pharmacokinetics and Safety Using Systems Pharmacology Nov 16, 2014 In-Person Instruction Japan Tokyo, Japan
    #7 Next Steps for Content of Company Core Data Sheet Prepared by Western Companies - Part 2 Nov 16, 2014 In-Person Instruction Japan Tokyo, Japan
    #8 An Introduction to Adaptive Designs Nov 16, 2014 In-Person Instruction Japan Tokyo, Japan
    #9 Let’s Learn and Talk about Project Management Basics of the Clinical Study in Medical Institutes! Nov 16, 2014 In-Person Instruction Japan Tokyo, Japan
    #10 HTA 2016? What are the challenges for Japan? Nov 16, 2014 In-Person Instruction Japan Tokyo, Japan
    Special DIA Japan 2014 Sunday Pass: Buy Pre-Conference Tutorial(s) and Stay for Afternoon Plenary/Special Sessions Nov 16, 2014 Meetings Japan Tokyo, Japan
    EudraVigilance - electronic reporting of ICSRs in the EEA Nov 17, 2014 In-Person Instruction Europe London, United Kingdom
    Special DIA Japan 2014 Medical Device Pass: Attend [V6-S6] and Stay through Closing Sessions Nov 18, 2014 Meetings Japan Tokyo, Japan
    Proarrhythmia Nov 19, 2014 ACPE, IACET Online Instruction Global Online
    eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) Nov 20, 2014 In-Person Instruction Europe London, United Kingdom
    FDA IND/NDA Workshop Nov 20, 2014 Meetings China Beijing, China
    Need to Reinvent the Clinical Trial? Innovate, Collaborate & Integrate Nov 20, 2014 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 1st DIA China Drug Induced Cardiovascular Toxicity Workshop Nov 23, 2014 Meetings China
    1st Maghreb Regulatory Conference Nov 24, 2014 Meetings Europe Algiers, Algeria
    ICH endorsed PhV training course Nov 26, 2014 In-Person Instruction Europe Algiers, Algeria
    EudraVigilance - electronic reporting of ICSRs in the EEA Nov 26, 2014 In-Person Instruction Europe Lisboa, Portugal
    Tutorial 01:ELECTRONIC TRIAL MASTER FILES (eTMF) - MOVING FROM IMPLEMENTATION TO PROJECT EXCELLENCE Dec 01, 2014 In-Person Instruction Europe Berlin, Germany
    Tutorial 02: UNDERSTANDING THE IMPACT OF IDENTIFICATION OF MEDICINAL PRODUCTS (IDMP) ON PROCESSES, DATA PROVISION, GOVERNANCE AND IT ARCHITECTURE Dec 01, 2014 In-Person Instruction Europe Berlin, Germany
    15th Annual Conference on Electronic Document Management (eDM) Dec 02, 2014 Meetings Europe Berlin, Germany
    Biosimilars Conference Dec 02, 2014 Meetings Europe Berlin, Germany
    Target Product Profile – Strategies to Optimize Drug Development, Product Labeling, and Commercialization Dec 02, 2014 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
    EudraVigilance - electronic reporting of ICSRs in the EEA Dec 03, 2014 In-Person Instruction Europe London, United Kingdom
    Facets of Drug-Induced Kidney Injury and Regulatory Perspective Dec 03, 2014 ACPE, IACET Online Instruction Global Online
    Cardio-Oncology: Innovative Strategies for Mitigating Cardiovascular Risk of New Cancer Therapies Dec 04, 2014 Online Instruction Global Online
    MHRA Information Day - MedDRA in the Pharmacovigilance Regulatory Process Dec 08, 2014 In-Person Instruction Europe London, United Kingdom
    Preparation of a Successful (CTD) with Quality by Design (QbD) Dec 08, 2014 In-Person Instruction China
    2nd DIA Advanced Regulatory Affairs Training Course in Japan Dec 08, 2014 In-Person Instruction Japan Tokyo, Japan
    3rd DIA Statistics Workshop for all Clinical Research Professionals in Japan Dec 09, 2014 Meetings Japan Tokyo, Japan
    Implementation and Status of Periodic Benefit-Risk Evaluation Reporting (PBRER) in Canada Dec 09, 2014 Online Instruction Global Online
    Pharmacovigilance and Risk Management Strategies 2015 Jan 26, 2015 Meetings North America Washington, DC, United States
    18th Annual Workshop in Japan for Clinical Data Management Jan 29, 2015 Meetings Japan Tokyo, Japan
    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: Drug/Device Marketing in an Evolving Environment Feb 17, 2015 Meetings North America Washington, DC, United States
    Benefit/Risk Management Mar 10, 2015 In-Person Instruction Europe Hamburg, Germany
    Essentials of European Regulatory Affairs Mar 10, 2015 In-Person Instruction Europe Hamburg, Germany
    3rd DIA Clinical Operation & Monitoring Workshop in Japan Mar 12, 2015 Meetings Japan Tokyo, Japan
    Medical & Scientific Communications 2015 Annual Forum Mar 16, 2015 Meetings North America Glendale, AZ, United States
    CMC Workshop 2015 Apr 13, 2015 Meetings North America Bethesda, MD, United States
    8th Annual Clinical Forum Apr 13, 2015 Meetings Europe Paris, France
    27th Annual EuroMeeting Apr 13, 2015 Meetings Europe Paris, France
    DIA/FDA Statistics Forum 2015 Apr 20, 2015 Meetings North America North Bethesda, MD, United States
    Global CTD Dossier – Regulatory aspects and focus on quality documentation including concepts of Quality by Design Apr 26, 2015 In-Person Instruction Europe Dakar, Senegal
    ICH endorsed PhV training course Apr 26, 2015 In-Person Instruction Europe Dakar, Senegal
    4th African Regulatory Conference (ARC) Apr 27, 2015 Meetings Europe Dakar, Senegal
    How to prepare for Pharmacovigilance Audits and Inspections Apr 28, 2015 In-Person Instruction Europe Basel, Switzerland
    eRegulatory and Intelligence Annual Conference May 11, 2015 Meetings North America
    7th DIA China Annual Meeting May 24, 2015 Meetings China Shanghai, China
    Medical Approach in Diagnosis and Management of ADRs Jun 10, 2015 In-Person Instruction Europe Charenton Le Pont, Paris, France
    Diagnosis and Management of Drug-Induced Liver Injury (DILI) Jun 11, 2015 In-Person Instruction Europe Charenton Le Pont, Paris, France
    DIA 2015 51st Annual Meeting: Develop. Innovate. Advance. Jun 14, 2015 Meetings North America Washington, DC, United States