|
|
|
|
|
|
|
|
|
|
|
|
|
|
 indicates items that take place in your region |
|
|
 Annual Meeting | |
|
|
 eLearning | |
|
Crisis Management - (Nov 20, 2008) - Online
|
Database Management - (Nov 20, 2008) - Online
|
Literature Evaluation - (Nov 20, 2008) - Online
|
Literature Searching - (Nov 20, 2008) - Online
|
Medical Inquires - (Nov 20, 2008) - Online
|
Medical Writing - (Nov 20, 2008) - Online
|
Product Labeling - (Nov 20, 2008) - Online
|
Regulatory Issues - (Nov 20, 2008) - Online
|
Navigating HIPAA: Module 1 - Overview and Administrative Simplification - (Nov 20, 2008) - Online
|
Navigating HIPAA: Module 2 - Privacy - (Nov 20, 2008) - Online
|
Navigating HIPAA: Module 3 - Security - (Nov 20, 2008) - Online
|
Navigating HIPAA: Module 4 - Electronic Transactions, Code Sets, and Unique Identifiers - (Nov 20, 2008) - Online
|
Clinical Investigator: Module 1 - Study Preparation and Initiation - (Nov 20, 2008) - Online
|
Clinical Investigator: Module 2 - Conducting The Study - (Nov 20, 2008) - Online
|
History of US Drug Regulation - (Nov 20, 2008) - Online
|
Informed Consent - (Nov 20, 2008) - Online
|
Statistics for Medical Communications Professionals - (Nov 20, 2008) - Online
|
SPL 1: Practical Overview of SPL and XML - (Nov 20, 2008) - Online
|
SPL 2: History, Business Case, and Solutions - (Nov 20, 2008) - Online
|
|
|
 EudraVigilance | |
|
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
|
Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Jan 07, 2009) - London
|
Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Jan 12, 2009) - London
|
Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Jan 28, 2009) - Prague 10
|
Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Feb 02, 2009) - London
|
Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Feb 25, 2009) - London
|
Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Mar 02, 2009) - London
|
EudraVigilance: Electronic Reporting of ICSRs in the EEA - (Mar 16, 2009) - Madrid
|
Eudravigilance - Electronic Reporting of ICSRs in the EEA - (Apr 06, 2009) - London
|
|
|
 Euro Meeting | |
|
|
 Meeting | |
|
5th Latin American Congress of Clinical Research: Regional Perspectives and Future Trends - (Nov 20, 2008) - Buenos Aires
|
European Regulatory Affairs Forum - (Nov 24, 2008) - Munich
|
9th Conference on European Electronic Document Management - (Dec 03, 2008) - Barcelona
|
3rd Annual Cardiac Safety Conference - (Dec 04, 2008) - Barcelona
|
User Testing workshop - (Dec 05, 2008)
|
DIA's 3rd Annual Conference on Drug Discovery and Clinical Development in India: Scientific, Regulatory, and Social Frontiers - (Dec 07, 2008) - Mumbai
|
Safety is Global: Contemporary Pharmacovigilance and Medical Product Risk Management Strategies - (Dec 10, 2008) - Singapore
|
8th Annual DIA Conference for Contemporary Pharmacovigilance and Risk Management Strategies - (Jan 11, 2009) - Washington
|
8th Middle East Regulatory Conference - MERC 2009 - (Jan 20, 2009)
|
12th Annual Workshop in Japan for CLINICAL DATA MANAGEMENT: Who should Be "Superman" in CDM? - (Jan 29, 2009) - Tokyo
|
Comparability Challenges: Regulatory and Scientific Issues in the Assessment of Biopharmaceuticals - (Feb 03, 2009) - Arlington
|
22nd Annual DIA Conference for Electronic Document Management: Addressing Challenges in an Electronic World - (Feb 10, 2009) - Philadelphia
|
CMC Regulatory and Technical Strategies: Global CMC Dossier Life Cycle Management - (Feb 16, 2009) - Bethesda
|
21st Annual DIA Conference on Marketing Pharmaceuticals in a Time of Change - (Feb 23, 2009) - New York
|
20th Annual Workshop on Medical Communications PAST, PRESENT, AND FUTURE - (Mar 01, 2009) - Hilton Head Island
|
24th Annual DIA DATA Conference and Exhibition: CLINICAL DATA LIFECYCLE Trial Design through Submission and Beyond - (Mar 09, 2009) - Philadelphia
|
The 3rd Annual FDA/DIA Statistics Forum - (Apr 26, 2009) - Arlington
|
QT, Arrhythmia, and Cardiovascular Safety Issues in Drug Development - (Apr 29, 2009) - Bethesda
|
6th EudraVigilance Information Day - (Jul 01, 2009) - London
|
|
|
 Training Course | |
|
Practical Considerations in Drug Development - (Dec 08, 2008) - Phoenix
|
Practical Guide for Pharmacovigilance: Clinical Trials and Post Marketing - (Dec 08, 2008) - Boulogne-Billancourt (Paris)
|
Regulatory Affairs: Part I:The IND Phase and Part II: The CTD/NDA Phase - (Jan 11, 2009) - Irvine
|
European Regulatory Affairs - (Jan 26, 2009) - San Francisco
|
Clinical Project Management - (Feb 09, 2009) - Baltimore
|
Excellence in Pharmacovigilance: Clinical Trials and Post Marketing - (Feb 09, 2009) - Paris
|
Development of a Clinical Study Report - (Feb 10, 2009) - Philadelphia
|
Essentials of Clinical Study Management - (Feb 18, 2009) - Madrid
|
European Regulatory Affairs - (Feb 18, 2009) - Nice
|
Building the eCTD - (Feb 19, 2009) - Madrid
|
The Leadership Experience - (Mar 02, 2009) - Atlanta
|
Clinical Statistics for Nonstatisticians - (Mar 02, 2009) - Philadelphia
|
Fundamentals of Clinical Research Monitoring - (Mar 09, 2009) - Philadelphia
|
Overview of Drug Development - (Mar 16, 2009) - Philadelphia
|
Regulatory Affairs Part I: The IND Phase - (Mar 23, 2009) - Baltimore
|
Regulatory Affairs Part I: The IND Phase and Part II: The CTD/NDA Phase - (Apr 27, 2009) - ATLANTA
|
The Leadership Experience - (May 04, 2009) - San Francisco
|
An Introduction to Product Information Management (PIM) - (May 14, 2009) - London
|
Regulatory II: The CTD/NDA Phase - (May 20, 2009) - Baltimore
|
European Regulatory Affairs - (Jun 11, 2009) - Amsterdam
|
Overview of Drug Development - (Aug 17, 2009) - Philadelphia
|
Medical Approach in Diagnosis and Management of ADRs - (Sep 17, 2009)
|
Excellence in Pharmacovigilance: Clinical Trials and Post Marketing - (Oct 12, 2009) - Berlin
|
An Introduction to Product Information Management (PIM) - (Oct 15, 2009) - Berlin
|
US Regulatory Affairs - (Oct 19, 2009) - Basel
|
Overview of Drug Development - (Nov 13, 2009) - Baltimore
|
|
|
 Tutorial | |
|
|
 Webinar | |
|
New! Three-part Online Training Series: Overview of Drug Development from Discovery through Marketing Application - (Dec 01, 2008) - Online
|
NEW! Three-Part Online Training Series: Who's Monitoring the Monitor? - (Dec 01, 2008) - Online
|
FDA and Industry Perspectives on Signal Detection and Data Mining - (Dec 04, 2008) - Online
|
Special Three-Part Online Training Series: Development of a Clinical Study Report - (Dec 08, 2008) - Online
|
Surefire Tactics for Recruiting Difficult Patient Populations - (Dec 11, 2008) - Online
|
Tools Used by Medical Science Liaisons, Involvement in Clinical Trials and Career Strategies: How does Your Company Compare? - (Dec 12, 2008) - Online
|
Electronic Data Capture: Strategies to Enhance Data Capture, Site Satisfaction and Study Participation - (Jan 14, 2009) - Online
|
FDAAA Legislation: Risk Evaluation and Mitigation Strategies (REMS) - (Jan 22, 2009) - Online
|
|
|
 Webinar Archive | |
|
ARCHIVED - Regulatory Requirements for Conducting Clinical Trials in India - (Nov 20, 2008) - Online
|
ARCHIVED - Outsourcing: Planning and Managing the Sponsor-provider Relationship - (Nov 20, 2008) - Online
|
ARCHIVED - Structured Product Labeling Release Four: electronic Drug Establishment Registration & Drug Listing - (Nov 20, 2008) - Online
|
Archived - The Evolving role of Project and Alliance Managers at Each Stage of Product Development - (Nov 20, 2008) - Online
|
Archived - Proven Strategies for Global Recruitment - (Nov 20, 2008) - Online
|
ARCHIVED - Recruitment Budget Planning - (Nov 20, 2008) - Online
|
ARCHIVED - Risk Management Strategies and Pharmacovigilance of Opioids and Other Controlled Substances - (Nov 20, 2008) - Online
|
Archived - Creating a Value Proposition for the Potential Participant and Their Family - (Nov 20, 2008) - Online
|
ARCHIVED - Are You Prepared for eCTD Submission? - (Nov 20, 2008) - Online
|
ARCHIVED - Clinical Data Acquisition Standards Harmonization (CDASH) Initiative - (Nov 20, 2008) - Online
|
Archived - Defining and Managing Protocol Deviation/Violation/Exception - (Nov 20, 2008) - Online
|
Archived - FDA Update and Overview of Proposed Pregnancy/Lactation Labeling Rule for Prescription Drugs and Biologics (Presented November 3, 2008) - (Nov 20, 2008) - Online
|
ARCHIVE - Special Two-Part Webinar Series: Best Practices for Preparing Standard Operating Procedures (SOPs) - (Nov 20, 2008) - Online
|
ARCHIVED - Essential First Steps to FDA 505(b)(2) Drug Approval - (Nov 20, 2008) - Online
|
Archived - FDA 505(b)(2) Patent and Exclusivity - (Nov 20, 2008) - Online
|
ARCHIVED - How Pharmacovigilance Audits Can Ensure Regulatory Compliance - (Nov 20, 2008) - Online
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|