|
|
|
|
|
|
|
|
|
 indicates items that take place in your region |
|
|
 Annual Meeting | |
|
|
 eLearning | |
|
SPL 1: Practical Overview of SPL and XML - (May 17, 2008) - Online
|
SPL 2: History, Business Case, and Solutions - (May 17, 2008) - Online
|
Crisis Management - (May 17, 2008) - Online
|
Database Management - (May 17, 2008) - Online
|
Literature Evaluation - (May 17, 2008) - Online
|
Literature Searching - (May 17, 2008) - Online
|
Medical Inquires - (May 17, 2008) - Online
|
Medical Writing - (May 17, 2008) - Online
|
Product Labeling - (May 17, 2008) - Online
|
Regulatory Issues - (May 17, 2008) - Online
|
Navigating HIPAA: Module 1 - Overview and Administrative Simplification - (May 17, 2008) - Online
|
Navigating HIPAA: Module 2 - Privacy - (May 17, 2008) - Online
|
Navigating HIPAA: Module 3 - Security - (May 17, 2008) - Online
|
Navigating HIPAA: Module 4 - Electronic Transactions, Code Sets, and Unique Identifiers - (May 17, 2008) - Online
|
Clinical Investigator: Module 1 - Study Preparation and Initiation - (May 17, 2008) - Online
|
Clinical Investigator: Module 2 - Conducting The Study - (May 17, 2008) - Online
|
History of US Drug Regulation - (May 17, 2008) - Online
|
Informed Consent - (May 17, 2008) - Online
|
Statistics for Medical Communications Professionals - (May 17, 2008) - Online
|
|
|
 EudraVigilance | |
|
Eudravigilance - Electronic Reporting of ICSRs in the EEA - (May 21, 2008) - London
|
EudraVigilance: Medicinal Product Dictionary - (Jun 10, 2008) - London
|
Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Jun 11, 2008) - London
|
Electronic Reporting of ICSRs & EudraVigilance - (Aug 18, 2008) - Horsham
|
Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Aug 27, 2008) - London
|
EudraVigilance: Medicinal Product Dictionary - (Sep 16, 2008) - London
|
Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Sep 17, 2008) - London
|
Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Sep 22, 2008) - London
|
EudraVigilance: Medicinal Product Dictionary - (Oct 14, 2008) - London
|
Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Oct 15, 2008) - London
|
Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Oct 20, 2008) - London
|
Electronic Reporting of ICSRs & EudraVigilance - (Nov 10, 2008) - Horsham
|
Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Nov 19, 2008) - London
|
Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Nov 24, 2008) - London
|
EudraVigilance: Medicinal Product Dictionary - (Nov 27, 2008) - London
|
Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Dec 10, 2008) - London
|
|
|
 Euro Meeting | |
|
|
 Meeting | |
|
Harmonisation for CLINICAL RESEARCH and DRUG DEVELOPMENT in the LATIN AMERICAN Region - (May 19, 2008) - Mexico City
|
FDA/DIA Co-sponsored Conference on The Orphan Drug Act (ODA) at 25 Years: Retrospective and Future Views - (May 19, 2008)
|
Emerging REGULATORY Issues in Genomic Medicine - (May 21, 2008) - Mexico City
|
EudraVigilance Information Day - (Jun 27, 2008) - London
|
Computerized Systems in Clinical Research: Current Quality and Data Integrity Concepts - (Sep 08, 2008) - Horsham
|
Immunogenicity of Therapeutic Proteins - (Sep 10, 2008) - Bethesda
|
EVIDENCE-BASED MEDICINE AND HEALTH TECHNOLOGY ASSESSMENT: Can We Find Common Ground? - (Sep 22, 2008) - Alexandria
|
2nd DIA Conference: Oligonucleotides-based Therapeutics - (Sep 22, 2008) - Falls Church
|
Innovation Forum - (Sep 29, 2008) - London
|
EudraVigilance Information Day - (Oct 06, 2008) - London
|
2nd Annual Clinical Forum - Data Driven Drug Development Decisions - (Oct 20, 2008) - Ljubljana
|
3rd Annual DIA Outsourcing Summit - (Oct 23, 2008) - Washington
|
Project Management Excellence in Life Sciences: Balancing Art and Science - (Oct 23, 2008) - Ljubljana
|
Project Management Excellence in Life Sciences: Balancing Art and Science - (Oct 23, 2008) - Washington
|
2 nd Paediatrics Forum - (Oct 30, 2008) - London
|
Pharmaceutical Patents and Regulatory Exclusivity Workshop - (Oct 30, 2008) - London
|
The 7th Annual Electronic Submissions Conference ECTD: The Adventure Continues - (Nov 05, 2008) - San Diego
|
DIA's 6th Canadian Annual Meeting: Benefit and Risk Management: An Evolution in Progress - (Nov 05, 2008) - Ottawa,
|
Regulatory Affairs Forum - (Nov 24, 2008) - Munich
|
9th Conference on European Electronic Document Management - (Dec 04, 2008) - Barcelona
|
Cardiac Safety - (Dec 04, 2008) - Barcelona
|
8th Middle East Regulatory Conference - (Jan 20, 2009) - Doha
|
|
|
 Training Course | |
|
Project Information, Communication, and Knowledge Management - (May 19, 2008) - Horsham
|
European Regulatory Affairs - (May 19, 2008) - Horsham
|
European Regulatory Affairs - (Jun 09, 2008) - Ljubljana
|
Regulatory Affairs: Part I: The IND Phase, Part II: The CTD/NDA Phase - (Aug 04, 2008) - Boston
|
Resource Management at the Functional and Enterprise Levels - (Aug 04, 2008) - Horsham
|
Project Risk Management - (Aug 11, 2008) - Horsham
|
Overview of Drug Development in Japan - (Aug 11, 2008) - Bethesda
|
Overview of Drug Development - (Aug 18, 2008) - Philadelphia
|
European Regulatory Affairs - (Aug 25, 2008) - Chicago
|
Building the eCTD - (Sep 08, 2008) - Prague
|
Clinical Statistics For Nonstatisticians - (Sep 08, 2008) - Washington
|
Drug Safety Surveillance And Epidemiology - (Sep 08, 2008) - Washington
|
Fundamentals of Clinical Research Monitoring - (Sep 15, 2008) - Washington
|
The Leadership Experience - (Sep 15, 2008) - Chicago
|
Regulatory I: The IND Phase - (Sep 15, 2008) - Philadelphia
|
Clinical Project Management - (Sep 15, 2008) - Horsham
|
Medical Approach in Diagnosis and Management of ADRs - (Sep 22, 2008) - Boulogne-Billancourt (Paris)
|
Essentials of Clinical Study Management - (Sep 22, 2008) - Boulogne-Billancourt (Paris)
|
European Regulatory Affairs - (Sep 25, 2008) - Frankfurt am Main
|
Team Building and Dynamics - (Oct 06, 2008) - Horsham
|
Excellence in Pharmacovigilance: Clinical Trials and Post Marketing - (Oct 13, 2008) - Barcelona
|
An Introduction to Product Information Management (PIM) - (Oct 13, 2008) - Barcelona
|
Essentials of Project Management - (Oct 13, 2008) - Phoenix
|
Advanced Clinical Statistics For Nonstatisticians - (Oct 13, 2008) - Horsham
|
Practical GCP Compliance Auditing of Trials & Systems - (Oct 15, 2008) - London
|
Portfolio, Strategy and Value Management - (Oct 16, 2008) - Phoenix
|
Regulatory Affairs Part II: The CTD/NDA Phase - (Oct 20, 2008) - Philadelphia
|
Introduction to Good Clinical Practices and Auditing - (Oct 20, 2008) - Del Mar
|
Introduction to Regulatory Affairs - (Oct 26, 2008) - Dubai
|
Project Information, Communication, and Knowledge Management - (Oct 27, 2008) - Horsham
|
New Drug Product Development and Lifecycle Management - (Oct 29, 2008) - Horsham
|
Preclinical Safety Sciences - (Nov 03, 2008) - Copenhagen
|
Clinical Statistics for NonStatisticians - (Nov 03, 2008) - Vienna
|
Essentials of Clinical Study Management - (Nov 05, 2008) - Vienna
|
Special Training Course on US Regulatory Affairs - (Nov 10, 2008) - Copenhagen
|
The Leadership Experience - (Nov 10, 2008) - Phoenix
|
Overview of Drug Development - (Nov 10, 2008) - Bethesda
|
European Regulatory Affairs - (Nov 10, 2008) - Washington
|
Regulatory Affairs: Part I: The IND Phase, Part II: The CTD/NDA Phase - (Nov 17, 2008) - Baltimore
|
Executing And Controlling Projects - (Nov 17, 2008) - Philadelphia
|
European Regulatory Affairs - (Nov 17, 2008) - Paris la Défence Cédex
|
Preclinical Safety Sciences - (Nov 24, 2008) - Dubai
|
Practical Considerations in Drug Development - (Dec 08, 2008) - Phoenix
|
|
|
 Tutorial | |
|
Tutorial #31: A Day in the Life of Adverse Event Reporting for Different Regions - (Jun 21, 2008) - Boston
|
Tutorial #32: Getting Your Clinical Operations on the Right Track: Strategy, Knowledge, People and Process - (Jun 21, 2008) - Boston
|
Tutorial #33: How to Prepare for an FDA GCP Audit - (Jun 21, 2008) - Boston
|
Tutorial #34: Regulatory Affairs in the European Union: An Overview of Registration Procedures for Medicinal Products in EU - (Jun 21, 2008) - Boston
|
Tutorial #35: Abuse Potential and Drug Dependence Assessment: Scientific and Regulatory Guidance in Drug Development - (Jun 21, 2008) - Boston
|
Tutorial #50: Planning and Conducting Clinical Trials in Oncology - (Jun 22, 2008)
|
Tutorial #53: Pharmacovigilance Assessment and Risk Management: Essential Components to Good Pharmacovigilance Practice - (Jun 22, 2008) - Boston
|
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
|
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
|
Tutorial #58: Structured Product Labeling Listing Data Elements Tutorial - (Jun 22, 2008) - Boston
|
Tutorial #59: Introduction to the PSUR: Pharmacovigilance and Medical Writing Perspectives - (Jun 22, 2008) - Boston
|
Tutorial #61: A Device Primer: IDEs, 510(k)s, PMAs, and Beyond - (Jun 22, 2008) - Boston
|
Tutorial #62: Leadership: How to Organize and Lead People in Group Work - (Jun 22, 2008) - Boston
|
Tutorial #63: Fourteen Steps from Research to Development - (Jun 22, 2008) - Boston
|
Tutorial #64: Comparability of Biopharmaceuticals - (Jun 22, 2008) - Boston
|
Tutorial #40: Regulatory Requirements for the Conduct of Clinical Trials in Europe - (Jun 22, 2008) - Boston
|
Tutorial #41: Clinical Statistics for Nonstatisticians - (Jun 22, 2008) - Boston
|
Tutorial #42: Principles of Safety Surveillance - (Jun 22, 2008) - Boston
|
Tutorial #43: Excelling as a Supervisor or Manager in the Clinical Research Industry - (Jun 22, 2008) - Boston
|
Tutorial #44: Managing Regulatory GCP Inspections - (Jun 22, 2008) - Boston
|
Tutorial #77: CTD Preparation: Module 2 Clinical Overview and Clinical Summary and Relationship to ISE and ISS - (Jun 22, 2008) - Boston
|
Tutorial #78: Project Management for the Nonproject Manager - (Jun 22, 2008) - Boston
|
Tutorial #79: Japan Regulatory Environment: Overview of the Organization, Processes, Systems, and Changes Affecting Pharmaceutical Development - (Jun 22, 2008) - Boston
|
Tutorial #70: Analysis of Safety Data from Clinical Trials - (Jun 22, 2008) - Boston
|
Tutorial #71: Evaluation of Risk Management Programs Using Existing Databases - (Jun 22, 2008) - Boston
|
Tutorial #73: The Creation and Management of a Worldwide Pharmacovigilance Quality Assurance Unit - (Jun 22, 2008) - Boston
|
Tutorial #75: GCP Issues in Emerging Regions: India, China - (Jun 22, 2008) - Boston
|
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)
|
Tutorial #81 Adaptive (Flexible) Trial Designs - (Jun 22, 2008) - Boston
|
|
|
 Webinar | |
|
|
 Webinar Archive | |
|
ARCHIVED FDA's Vision for Interactions with counterpart Regulators Around the World - (May 17, 2008) - Online
|
ARCHIVED Achieving Value in Your Company-sponsored Clinical Trial - (May 17, 2008) - Online
|
ARCHIVED Benefits of Data Standardization for the Pharmaceutical Industry - (May 17, 2008) - Online
|
ARCHIVED - Essential First Steps to FDA 505(b)(2) Drug Approval - (May 17, 2008) - Online
|
ARCHIVED - SUSAR's in the EEA - (May 17, 2008) - Online
|
ARCHIVED - How Pharmacovigilance Audits Can Ensure Regulatory Compliance - (May 17, 2008) - Online
|
ARCHIVED - Designing a Global Strategic Recruitment and Retention Plan - (May 17, 2008) - Online
|
ARCHIVED - Pandemic Influenza: Is Your Company Ready to Cope? - (May 17, 2008) - Online
|
Archived - FDA 505(b)(2) Patent and Exclusivity - (May 17, 2008) - Online
|
Archived - Three Key Aspects of Risk Management During Phase 3 Clinical Trials - (May 17, 2008) - Online
|
Archived - Site and Sponsor Recruitment Preparations Prior to the Investigator Meeting - (May 17, 2008) - Online
|
Companion to the FDA Pharmacogenomics Guidance - (May 17, 2008) - Online
|
ARCHIVED - Signal Investigation: Taking Pharmacovigilance Data Mining Beyond Signal Detection - (May 17, 2008) - Online
|
ARCHIVED - Using Dynamic Enrollment Management to Reduce Enrollment Cycle Time Variance - (May 17, 2008) - Online
|
ARCHIVED WEBINAR - Proven Strategies for compliant Clinical Trial Results Disclosure - (May 17, 2008) - Online
|
ARCHIVE - Volume 9A of the Rules Governing Medicinal Products in the European Union: What Does It All Mean? Part 2 - (May 17, 2008) - Online
|
| ARCHIVED WEBINAR - General Issues in Safety Assessment of Oligonucleotide-based Therapeutics, Parts 1 and 2 - (May 17, 2008) - Online | | | | | |