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 indicates items that take place in your region |
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 Annual Meeting | |
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 eLearning | |
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Crisis Management - (Jul 04, 2009) - Online
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Database Management - (Jul 04, 2009) - Online
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Literature Evaluation - (Jul 04, 2009) - Online
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Literature Searching - (Jul 04, 2009) - Online
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Medical Inquires - (Jul 04, 2009) - Online
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Medical Writing - (Jul 04, 2009) - Online
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Product Labeling - (Jul 04, 2009) - Online
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Regulatory Issues - (Jul 04, 2009) - Online
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Clinical Investigator: Module 1 - Study Preparation and Initiation - (Jul 04, 2009) - Online
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Clinical Investigator: Module 2 - Conducting The Study - (Jul 04, 2009) - Online
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History of US Drug Regulation - (Jul 04, 2009) - Online
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Informed Consent - (Jul 04, 2009) - Online
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Statistics for Medical Communications Professionals - (Jul 04, 2009) - Online
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 EudraVigilance | |
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Jul 15, 2009) - London
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Jul 20, 2009) - London
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Aug 26, 2009) - London
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Sep 02, 2009) - London
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Sep 07, 2009) - London
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EudraVigilance: Medicinal Product Dictionary - (Sep 10, 2009) - London
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EudraVigilance: Electronic Reporting of ICSRs in the EEA - (Sep 23, 2009) - Lisboa
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Oct 05, 2009) - London
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EudraVigilance - Electronic Reporting of ICSRs in the EEA - (Oct 21, 2009) - Vienna
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Eudravigilance Information Day - (Nov 04, 2009) - London
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Nov 04, 2009) - London
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Nov 09, 2009) - London
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EudraVigilance - Electronic Reporting of ICSR's in the EEA - (Nov 16, 2009) - Horsham
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EudraVigilance: Electronic Reporting of ICSRs in the EEA - (Nov 25, 2009) - Paris
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Dec 07, 2009) - London
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EudraVigilance: Medicinal Product Dictionary - (Dec 10, 2009) - London
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Jan 18, 2010) - London
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Feb 17, 2010) - London
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Mar 03, 2010) - London
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Mar 17, 2010) - London
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Apr 12, 2010) - London
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Apr 26, 2010) - London
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (May 17, 2010) - London
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (May 26, 2010) - London
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Jun 09, 2010) - London
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Jun 14, 2010) - London
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Jul 05, 2010) - London
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Sep 01, 2010) - London
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Sep 15, 2010) - London
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Oct 13, 2010) - London
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Oct 20, 2010) - London
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Nov 10, 2010) - London
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Nov 17, 2010) - London
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Dec 15, 2010) - London
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 Euro Meeting | |
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 Meeting | |
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eDrug Listing and Establishment Registration FDA and Industry: Overview and Lessons Learned on SPL - (Aug 11, 2009) - Philadelphia
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Cardiovascular Safety and Development of Type 2 Diabetes Mellitus Medications: Current State of the Art and Opportunities to Advance the Science - (Sep 23, 2009) - Washington
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6th LATIN AMERICAN CONGRESS OF CLINICAL RESEARCH Current Innovations, Opportunities, and Challenges - (Sep 23, 2009) - Mexico City
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DIA Biosimilars Workshop 2009 - (Sep 28, 2009) - London
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3rd Annual Clinical Trials Registries and Results Databanks: Recipe for Success - (Oct 06, 2009) - National Harbor
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DIA/FDA/NCI/PhRMA Progression-Free Survival Oncology Workshop - (Oct 07, 2009) - Bethesda
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Personalized Medicine: Biomarkers and Diagnostics in Drug Development, Regulatory Approval, and Access to Patients - (Oct 15, 2009) - Toronto
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3rd Annual Clinical Forum - (Oct 19, 2009) - Nice
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The 6th Multitrack Workshop in Japan - (Oct 22, 2009) - Tokyo
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DIA/EMEA/CMD(h) joint Conference on Variations - (Oct 26, 2009) - London
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Measuring Study Endpoints in Multinational Clinical Trials: Outcomes Reported from the Viewpoint of the Clinician, Patient, and Caregiver - (Oct 26, 2009) - New Orleans
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3rd Paediatric Forum EFGCP Children's Medicines Working Party 5th Annual Conference - (Oct 27, 2009) - London
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DIA/FDA/PhRMA Modeling and Simulation in Drug Development: Quantitative Approaches for Decision Making - (Oct 28, 2009) - Bethesda
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DIA's 7th Annual Canadian Meeting: Time to Act - (Nov 03, 2009) - Ottawa
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Assessing Benefits and Risks of Medicinal Products in Regulatory Decisions - (Nov 03, 2009) - Bethesda
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Global Vaccine Development for World Health Symposium/FDA, EMEA, Emerging Regions, NGO, and Industry Perspectives - (Nov 03, 2009) - North Bethesda
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Pharmaceutical Quality Forum - (Nov 09, 2009) - Prague
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The 8th Annual Electronic Submissions Conference; eCTD: The Adventure Continues - (Nov 17, 2009) - San Diego
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2nd Latin American Regulatory Conference (LARC) - Harmonization for Clinical Research and Drug Development in the Latin American Region - (Nov 18, 2009) - Mexico City
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DIA Health Technology Assessment Forum - (Nov 25, 2009) - Paris
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10th Conference on European Electronic Document Management - (Dec 02, 2009) - Vienna
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23rd Annual DIA Conference for Electronic Document Management: Global Content Management in an Electronic World - (Feb 03, 2010)
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EudraVigilance: Medicinal Product Dictionary - (Feb 16, 2010) - London
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Evidence Based Medicine & Health Tehcnology Assessment: Moving From Separate Appraisals to Synergistic Communications - (Mar 01, 2010)
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EudraVigilance: Medicinal Product Dictionary - (May 25, 2010) - London
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EudraVigilance: Medicinal Product Dictionary - (Sep 14, 2010) - London
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EudraVigilance: Medicinal Product Dictionary - (Nov 09, 2010) - London
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 Training Course | |
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Introduction to Signal Detection and Data Mining - (Aug 03, 2009) - Horsham
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Regulatory Affairs: Part I: The IND Phase & Part II: The CTD/NDA Phase - (Aug 03, 2009) - Boston
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How to Prepare for a Safety Inspection - (Aug 04, 2009) - Horsham
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Overview of Drug Development in Japan - (Aug 13, 2009) - Horsham
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Overview of Drug Development - (Aug 17, 2009) - Philadelphia
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Executing and Controlling Projects - (Aug 18, 2009) - Horsham
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Project Risk Management - (Aug 20, 2009) - Horsham
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European Regulatory Affairs - (Aug 24, 2009) - Denver
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Clinical Statistics for Nonstatisticians - (Sep 10, 2009) - Baltimore
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European Regulatory Affairs - (Sep 10, 2009) - Frankfurt am Main
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Regulatory I: The IND Phase - (Sep 14, 2009) - Philadelphia
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Essentials of Clinical Study Management - (Sep 16, 2009) - Copenhagen
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Building the eCTD - (Sep 17, 2009) - Copenhagen
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Medical Approach in Diagnosis and Management of ADRs - (Sep 17, 2009) - Boulogne-Billancourt (Paris)
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The Leadership Experience - (Sep 21, 2009) - Philadelphia
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High Performance Biopharm Teams - (Sep 22, 2009) - Horsham
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Fundamentals of Clinical Research Monitoring - (Sep 22, 2009) - Baltimore
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Drug Safety Surveillance and Epidemiology - (Sep 22, 2009) - Baltimore
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Clinical Project Management in Europe - Part I - (Sep 23, 2009) - Prague
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New Drug Product Development and Lifecycle Management - (Sep 24, 2009) - Horsham
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Practical GCP Compliance Auditing of Trials & Systems - (Oct 07, 2009) - London
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Clinical Statistics for Nonstatisticians - (Oct 08, 2009) - London
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Advanced Clinical Statistics for Nonstatisticians - (Oct 08, 2009) - Horsham
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Excellence in Pharmacovigilance: Clinical Trials and Post Marketing - (Oct 12, 2009) - Berlin
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Practical Considerations in Drug Development - (Oct 14, 2009) - Horsham
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An Introduction to Product Information Management (PIM) - (Oct 15, 2009) - Berlin
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Special Training Course on US Regulatory Affairs - (Oct 19, 2009) - Basel
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Project Information, Communication and Knowledge Management - (Oct 19, 2009) - Horsham
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Regulatory Affairs Part II: The CTD/NDA Phase - (Oct 19, 2009) - Philadelphia
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Essentials of Project Management - (Oct 21, 2009) - Horsham
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Clinical Project Management - (Oct 26, 2009) - Philadelphia
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CTD Dossier Requirements: Focus on EU Module 1 and Quality Module 3 - (Nov 01, 2009) - Dubai
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Regulatory Affairs: Part I: The IND Phase & Part II: The CTD/NDA Phase - (Nov 02, 2009) - Baltimore
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Introduction to Good Clinical Practices and Auditing - (Nov 02, 2009) - Baltimore
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Introduction to Portfolio Management and Performance Metrics - (Nov 04, 2009) - Horsham
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The Leadership Experience - (Nov 09, 2009) - Dallas
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European Regulatory Affairs: An in-depth Review of Registration Procedures in the European Union - (Nov 09, 2009) - Washington
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Overview of Drug Development - (Nov 13, 2009) - Baltimore
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Enterprise Resource Planning - (Nov 17, 2009) - Horsham
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Practical Guide for Pharmacovigilance: Clinical Trials and Post Marketing - (Nov 18, 2009) - Boulogne-Billancourt (Paris)
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European Regulatory Affairs - (Nov 19, 2009) - Boulogne-Billancourt (Paris)
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Non-Clinical Safety Sciences and Their Regulatory Aspects - (Nov 23, 2009) - Lisbon
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Essentials of Clinical Study Management - (Dec 02, 2009) - Basel
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Computer Systems Validation for the Non-computer Professional - (Dec 02, 2009) - Horsham
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Utilizing Chemistry, Manufacturing & Control in Drug Development - (Dec 03, 2009) - Horsham
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How to Prepare for a Safety Inspection - (Dec 07, 2009) - Horsham
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Introduction to Signal Detection and Data Mining - (Dec 08, 2009) - Horsham
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Comprehensive Training on European Regulatory Affairs: Expert Overview - (Jan 24, 2010) - Dubai
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Clinical Project Management in Europe – Part II - (Feb 10, 2010) - Paris
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 Tutorial | |
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 Webinar | |
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Clinical Statistics for Nonstatisticians - 5 Part On-line Training Series - (Jul 13, 2009) - Online
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Opioids: Current Perspective and Challenges from Phase 3 to REMS - (Jul 14, 2009) - Online
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Basics of an IND - 6 Part On-line Training Series - (Jul 14, 2009) - Online
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Clinical Trial Landscape in India Webinar Series – Part 1 -Worldwide Regulatory Landscape: Current Regulatory Initiatives in the US, Canada and EU - (Jul 15, 2009) - Online
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Pre-marketing Strategies for Central Nervous Systems (CNS) Drugs - (Jul 20, 2009) - Online
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How Strategic Partnerships Can Accelerate Pandemic Flu Vaccine Development - (Jul 21, 2009) - Online
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Clinical Trial Landscape in India Webinar Series – Part 2 -Ethical Issues in Clinical Trials in Individuals with Reduced Autonomy - (Jul 22, 2009) - Online
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Clinical Trial Landscape in India Webinar Series – Part 3 -Ethical Issues in Non-therapeutic Trials - (Jul 29, 2009) - Online
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Generic Biologics: Separating Science Fact from Science Fiction - (Aug 11, 2009) - Online
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Developing Standard Operating Procedures (SOPs) - 3-Part Online Training Series - (Sep 15, 2009) - Online
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Development of a Clinical Study Report - 3-Part On-line Training Series - (Sep 29, 2009) - Online
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Overview of Drug Development - 3-Part Online Training Series - (Sep 30, 2009) - Online
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Who's Monitoring the Monitor - 3-Part Online training Series - (Oct 05, 2009) - Online
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Good Clinical Practices for the Clinical Research Professional - 4 Part On-line Training Series - (Nov 09, 2009) - Online
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 Webinar Archive | |
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ARCHIVED - Regulated Product Submissions (RPS) Promise and Progress - (Jul 04, 2009) - Online
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ARCHIVED - European Guidance on Risk Management of Human Pharmaceuticals in Pregnancy and Lactation - (Jul 04, 2009) - Online
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Archived - Electronic Submission Gateway Update - (Jul 04, 2009) - Online
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ARCHIVED - Wyeth v. Levine: Understanding the U.S. Supreme Court's Recent Failure-to-Warn Preemption Case - (Jul 04, 2009) - Online
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ARCHIVED - FDA Discusses Sentinel Initiative - (Jul 04, 2009) - Online
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ARCHIVED - Overview of Meta-Analysis Including Analysis of Rare Adverse Event Data - META-ANALYSIS WEBINAR SERIES (Part 1) - (Jul 04, 2009) - Online
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ARCHIVED - META-Analysis of Observational Data - META-ANALYSIS WEBINAR SERIES (Part 2) - (Jul 04, 2009) - Online
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ARCHIVED - Role of Meta-Analysis in Regulatory Decision Making - META-ANALYSIS WEBINAR SERIES (Part 3) - (Jul 04, 2009) - Online
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ARCHIVED - Core Safety Profile and Labeling Harmonization in the European Union - (Jul 04, 2009) - Online
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Archived - Regulatory Strategies for Ensuring Compliance in Global Clinical Trials - (Jul 04, 2009) - Online
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Archived - Update on FDA's Good Importer Practices and Pharnaceutical Secure Supply-chain Pilot Program - (Jul 04, 2009) - Online
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Novel Approaches for Using Electronic Health Records for Pharmacovigilance - (Jul 04, 2009) - Online
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Archived - Pharmacovigilance Regulations in India - (Jul 04, 2009) - Online
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ARCHIVED-FDAAA Legislation Update: Risk Evaluation and Mitigation Strategies (REMS) - (Jul 04, 2009) - Online
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ARCHIVE - Cost-Effective Adverse Event Case Processing - (Jul 04, 2009) - Online
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ARCHIVED - Electronic Data Capture: Strategies to Enhance Data Capture, Site Satisfaction and Study Participation - (Jul 04, 2009) - Online
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ARCHIVED - FDA and Industry Perspectives on Signal Detection and Data Mining - (Jul 04, 2009) - Online
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Archived - Defining and Managing Protocol Deviation/Violation/Exception - (Jul 04, 2009) - Online
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ARCHIVED - Regulatory Requirements for Conducting Clinical Trials in India - (Jul 04, 2009) - Online
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ARCHIVED - Recruitment Budget Planning - (Jul 04, 2009) - Online
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ARCHIVED - Risk Management Strategies and Pharmacovigilance of Opioids and Other Controlled Substances - (Jul 04, 2009) - Online
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ARCHIVED - Outsourcing: Planning and Managing the Sponsor-provider Relationship - (Jul 04, 2009) - Online
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Archived - Proven Strategies for Global Recruitment - (Jul 04, 2009) - Online
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Archived - The Evolving role of Project and Alliance Managers at Each Stage of Product Development - (Jul 04, 2009) - Online
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ARCHIVED - Clinical Data Acquisition Standards Harmonization (CDASH) Initiative - (Jul 04, 2009) - Online
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Archived - FDA 505(b)(2) Patent and Exclusivity - (Jul 04, 2009) - Online
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The New Look at eCTD Lifecycle Management: How Mapping from NDA to IND can Streamline Submission Lifecycle Chores - (Jul 04, 2009) - Online
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ARCHIVED - How to Ensure Legally Admissible and Compliant Digital Signatures and Identities - (Jul 04, 2009) - Online
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ARCHIVED - Why You Need to Know About the EDM Reference Model - (Jul 04, 2009) - Online
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