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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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SPL 1: Practical Overview of SPL and XML - (May 09, 2008) - Online
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SPL 2: History, Business Case, and Solutions - (May 09, 2008) - Online
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Crisis Management - (May 09, 2008) - Online
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Database Management - (May 09, 2008) - Online
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Literature Evaluation - (May 09, 2008) - Online
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Literature Searching - (May 09, 2008) - Online
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Medical Inquires - (May 09, 2008) - Online
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Medical Writing - (May 09, 2008) - Online
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Product Labeling - (May 09, 2008) - Online
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Regulatory Issues - (May 09, 2008) - Online
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Navigating HIPAA: Module 1 - Overview and Administrative Simplification - (May 09, 2008) - Online
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Navigating HIPAA: Module 2 - Privacy - (May 09, 2008) - Online
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Navigating HIPAA: Module 3 - Security - (May 09, 2008) - Online
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Navigating HIPAA: Module 4 - Electronic Transactions, Code Sets, and Unique Identifiers - (May 09, 2008) - Online
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Clinical Investigator: Module 1 - Study Preparation and Initiation - (May 09, 2008) - Online
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Clinical Investigator: Module 2 - Conducting The Study - (May 09, 2008) - Online
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History of US Drug Regulation - (May 09, 2008) - Online
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Informed Consent - (May 09, 2008) - Online
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Statistics for Medical Communications Professionals - (May 09, 2008) - Online
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 EudraVigilance | |
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EudraVigilance - Electronic Reporting of ICSRs in the EEA - (May 14, 2008) - Paris
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (May 21, 2008) - London
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EudraVigilance: Medicinal Product Dictionary - (Jun 10, 2008) - London
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Jun 11, 2008) - London
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Electronic Reporting of ICSRs & EudraVigilance - (Aug 18, 2008) - Horsham
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Aug 27, 2008) - London
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EudraVigilance: Medicinal Product Dictionary - (Sep 16, 2008) - London
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Sep 17, 2008) - London
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Sep 22, 2008) - London
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EudraVigilance: Medicinal Product Dictionary - (Oct 14, 2008) - London
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Oct 15, 2008) - London
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Oct 20, 2008) - London
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Electronic Reporting of ICSRs & EudraVigilance - (Nov 10, 2008) - Horsham
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Nov 19, 2008) - London
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Nov 24, 2008) - London
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EudraVigilance: Medicinal Product Dictionary - (Nov 27, 2008) - London
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Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Dec 10, 2008) - London
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 Euro Meeting | |
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 Meeting | |
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Digital Signatures: Practical Strategies for Life Science Organizations - (May 13, 2008) - Arlington
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Harmonisation for CLINICAL RESEARCH and DRUG DEVELOPMENT in the LATIN AMERICAN Region - (May 19, 2008) - Mexico City
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FDA/DIA Co-sponsored Conference on The Orphan Drug Act (ODA) at 25 Years: Retrospective and Future Views - (May 19, 2008)
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Emerging REGULATORY Issues in Genomic Medicine - (May 21, 2008) - Mexico City
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EudraVigilance Information Day - (Jun 27, 2008) - London
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Computerized Systems in Clinical Research: Current Quality and Data Integrity Concepts - (Sep 08, 2008) - Horsham
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Immunogenicity of Therapeutic Proteins - (Sep 10, 2008) - Bethesda
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EVIDENCE-BASED MEDICINE AND HEALTH TECHNOLOGY ASSESSMENT: Can We Find Common Ground? - (Sep 22, 2008) - Alexandria
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2nd DIA Conference: Oligonucleotides-based Therapeutics - (Sep 22, 2008) - Falls Church
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Innovation Forum - (Sep 29, 2008) - London
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EudraVigilance Information Day - (Oct 06, 2008) - London
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2nd Annual Clinical Forum - Data Driven Drug Development Decisions - (Oct 20, 2008) - Ljubljana
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Project Management Excellence in Life Sciences: Balancing Art and Science - (Oct 23, 2008) - Washington
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Project Management Excellence in Life Sciences: Balancing Art and Science - (Oct 23, 2008) - Ljubljana
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3rd Annual DIA Outsourcing Summit - (Oct 23, 2008) - Washington
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2 nd Paediatrics Forum - (Oct 30, 2008) - London
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Pharmaceutical Patents and Regulatory Exclusivity Workshop - (Oct 30, 2008) - London
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DIA's 6th Canadian Annual Meeting: Benefit and Risk Management: An Evolution in Progress - (Nov 05, 2008) - Ottawa,
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Regulatory Affairs Forum - (Nov 24, 2008) - Munich
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9th Conference on European Electronic Document Management - (Dec 04, 2008) - Barcelona
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Cardiac Safety - (Dec 04, 2008) - Barcelona
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8th Middle East Regulatory Conference - (Jan 20, 2009) - Doha
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 Training Course | |
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Project Information, Communication, and Knowledge Management - (May 19, 2008) - Horsham
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European Regulatory Affairs - (May 19, 2008) - Horsham
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European Regulatory Affairs - (Jun 09, 2008) - Ljubljana
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Regulatory Affairs: Part I: The IND Phase, Part II: The CTD/NDA Phase - (Aug 04, 2008) - Boston
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Resource Management at the Functional and Enterprise Levels - (Aug 04, 2008) - Horsham
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Project Risk Management - (Aug 11, 2008) - Horsham
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Overview of Drug Development in Japan - (Aug 11, 2008) - Bethesda
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Overview of Drug Development - (Aug 18, 2008) - Philadelphia
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European Regulatory Affairs - (Aug 25, 2008) - Chicago
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Building the eCTD - (Sep 08, 2008) - Prague
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Clinical Statistics For Nonstatisticians - (Sep 08, 2008) - Washington
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Drug Safety Surveillance And Epidemiology - (Sep 08, 2008) - Washington
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Fundamentals of Clinical Research Monitoring - (Sep 15, 2008) - Washington
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The Leadership Experience - (Sep 15, 2008) - Chicago
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Clinical Project Management - (Sep 15, 2008) - Horsham
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Regulatory I: The IND Phase - (Sep 15, 2008) - Philadelphia
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Medical Approach in Diagnosis and Management of ADRs - (Sep 22, 2008) - Boulogne-Billancourt (Paris)
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Essentials of Clinical Study Management - (Sep 22, 2008) - Boulogne-Billancourt (Paris)
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European Regulatory Affairs - (Sep 25, 2008) - Frankfurt am Main
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Team Building and Dynamics - (Oct 06, 2008) - Horsham
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Excellence in Pharmacovigilance: Clinical Trials and Post Marketing - (Oct 13, 2008) - Barcelona
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An Introduction to Product Information Management - (Oct 13, 2008) - Barcelona
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Essentials of Project Management - (Oct 13, 2008) - Phoenix
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Advanced Clinical Statistics For Nonstatisticians - (Oct 13, 2008) - Horsham
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Practical GCP Compliance Auditing of Trials & Systems - (Oct 15, 2008) - London
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Portfolio, Strategy and Value Management - (Oct 16, 2008) - Phoenix
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Regulatory Affairs Part II: The CTD/NDA Phase - (Oct 20, 2008) - Philadelphia
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Introduction to Good Clinical Practices and Auditing - (Oct 20, 2008) - Del Mar
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Introduction to Regulatory Affairs - Module One - (Oct 26, 2008) - Dubai
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Project Information, Communication, and Knowledge Management - (Oct 27, 2008) - Horsham
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New Drug Product Development and Lifecycle Management - (Oct 29, 2008) - Horsham
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Clinical Statistics for NonStatisticians - (Nov 03, 2008) - Vienna
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Preclinical Safety Sciences - (Nov 03, 2008) - Copenhagen
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Essentials of Clinical Study Management - (Nov 05, 2008) - Vienna
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Special Training Course on US Regulatory Affairs - (Nov 10, 2008) - Copenhagen
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The Leadership Experience - (Nov 10, 2008) - Phoenix
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Overview of Drug Development - (Nov 10, 2008) - Bethesda
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European Regulatory Affairs - (Nov 10, 2008) - Washington
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Regulatory Affairs: Part I: The IND Phase, Part II: The CTD/NDA Phase - (Nov 17, 2008) - Baltimore
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Executing And Controlling Projects - (Nov 17, 2008) - Philadelphia
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European Regulatory Affairs - (Nov 17, 2008) - Paris la Défence Cédex
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Preclinical Safety Sciences - (Nov 24, 2008) - Dubai
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Practical Considerations in Drug Development - (Dec 08, 2008) - Phoenix
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 Tutorial | |
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Tutorial #31: A Day in the Life of Adverse Event Reporting for Different Regions - (Jun 21, 2008) - Boston
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Tutorial #32: Getting Your Clinical Operations on the Right Track: Strategy, Knowledge, People and Process - (Jun 21, 2008) - Boston
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Tutorial #33: How to Prepare for an FDA GCP Audit - (Jun 21, 2008) - Boston
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Tutorial #34: Regulatory Affairs in the European Union: An Overview of Registration Procedures for Medicinal Products in EU - (Jun 21, 2008) - Boston
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Tutorial #35: Abuse Potential and Drug Dependence Assessment: Scientific and Regulatory Guidance in Drug Development - (Jun 21, 2008) - Boston
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Tutorial #36: Financing of Pharmaceutical and Biotech Start-ups - (Jun 21, 2008) - Boston
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Tutorial #50: Planning and Conducting Clinical Trials in Oncology - (Jun 22, 2008)
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Tutorial #51: A Mapping Primer: The Use of Terminology Standards to Meet Regulatory and Interoperability Requirements - (Jun 22, 2008) - Boston
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Tutorial #53: Pharmacovigilance Assessment and Risk Management: Essential Components to Good Pharmacovigilance Practice - (Jun 22, 2008) - Boston
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Tutorial #55: Active Query, Case Assessment and Narrative Writing in Clinical Trials and Postmarketing Pharmacovigilance: Obtaining Quality Data through Clinical Expertise - (Jun 22, 2008) - Boston
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Tutorial #56: Clinical Research and Pharmaceutical Registration in India - (Jun 22, 2008) - Boston
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Tutorial #57: FDA Enforcement: Understanding the Agency's Authority. How Violations Occur, How to Prevent Them, and How to Respond if Violations Do Occur - (Jun 22, 2008) - Boston
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Tutorial #58: Structured Product Labeling Listing Data Elements Tutorial - (Jun 22, 2008) - Boston
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Tutorial #59: Introduction to the PSUR: Pharmacovigilance and Medical Writing Perspectives - (Jun 22, 2008) - Boston
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Tutorial #60: Understanding and Managing Uncertainty in Pharmaceutical and Biotech R&D - (Jun 22, 2008) - Boston
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Tutorial #61: A Device Primer: IDEs, 510(k)s, PMAs, and Beyond - (Jun 22, 2008) - Boston
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Tutorial #62: Leadership: How to Organize and Lead People in Group Work - (Jun 22, 2008) - Boston
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Tutorial #63: Fourteen Steps from Research to Development - (Jun 22, 2008) - Boston
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Tutorial #64: Comparability of Biopharmaceuticals - (Jun 22, 2008) - Boston
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Tutorial #41: Clinical Statistics for Nonstatisticians - (Jun 22, 2008) - Boston
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Tutorial #42: Principles of Safety Surveillance - (Jun 22, 2008) - Boston
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Tutorial #43: Excelling as a Supervisor or Manager in the Clinical Research Industry - (Jun 22, 2008) - Boston
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Tutorial #44: Managing Regulatory GCP Inspections - (Jun 22, 2008) - Boston
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Tutorial #45: Comparability: How to Manage the Impact of Process Change - (Jun 22, 2008) - Boston
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Tutorial #40: Regulatory Requirements for the Conduct of Clinical Trials in Europe - (Jun 22, 2008) - Boston
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Tutorial #76: Training Considerations for Patient-reported Outcomes - (Jun 22, 2008) - Boston
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Tutorial #77: CTD Preparation: Module 2 Clinical Overview and Clinical Summary and Relationship to ISE and ISS - (Jun 22, 2008) - Boston
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Tutorial #78: Project Management for the Nonproject Manager - (Jun 22, 2008) - Boston
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Tutorial #79: Japan Regulatory Environment: Overview of the Organization, Processes, Systems, and Changes Affecting Pharmaceutical Development - (Jun 22, 2008) - Boston
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Tutorial #80: Working Across Cultures: Asia and the West - (Jun 22, 2008) - Boston
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Tutorial #82: Who’s Monitoring the Monitor? Explore Trends, Management Techniques and a Reality-Check for Sponsors Utilizing CRO- and Alliance-based Site Monitoring - (Jun 22, 2008)
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Tutorial #81 Adaptive (Flexible) Trial Designs - (Jun 22, 2008) - Boston
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Tutorial #70: Analysis of Safety Data from Clinical Trials - (Jun 22, 2008) - Boston
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Tutorial #71: Evaluation of Risk Management Programs Using Existing Databases - (Jun 22, 2008) - Boston
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Tutorial #72: Effective Drug Safety Systems - (Jun 22, 2008) - Boston
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Tutorial #73: The Creation and Management of a Worldwide Pharmacovigilance Quality Assurance Unit - (Jun 22, 2008) - Boston
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Tutorial #74: Electronic Submission Success - (Jun 22, 2008) - Boston
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Tutorial #75: GCP Issues in Emerging Regions: India, China - (Jun 22, 2008) - Boston
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 Webinar | |
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 Webinar Archive | |
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ARCHIVED - Features and Benefits of FDA Data Exchange Standard Initiatives - (May 09, 2008) - Online
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ARCHIVED - Special Report on the Status of Behind-the-Counter Drugs - (May 09, 2008) - Online
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Companion to the FDA Pharmacogenomics Guidance - (May 09, 2008) - Online
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ARCHIVED WEBINAR - Are You Prepared for eCTD Submission - (May 09, 2008) - Online
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ARCHIVED WEBINAR - Modern Strategies to Combat Counterfeit Drugs - (May 09, 2008) - Online
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ARCHIVED WEBINAR - Learn the Whys and Hows of Medical Information Website Development - (May 09, 2008) - Online
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ARCHIVED WEBINAR - Proven Strategies for compliant Clinical Trial Results Disclosure - (May 09, 2008) - Online
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ARCHIVED - Registration with EudraVigilance: Procedures, Background and Commonly Encountered Issues - (May 09, 2008) - Online
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ARCHIVED - Prescription Drug Labeling: Update from the FDA Perspective - (May 09, 2008) - Online
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ARCHIVED - Signal Investigation: Taking Pharmacovigilance Data Mining Beyond Signal Detection - (May 09, 2008) - Online
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