CBI Announces FDA Participation at Upcoming Forum on Clinical Trial Investigator Portals
Jonathan Helfgott, Consumer Safety Officer, CDRH Division of Bioresearch Monitoring of the FDA, will join Munther Baara, Director, Clinical Business Systems and Processes, Wyeth Pharmaceuticals; Steve Sweeney, Head, Clinical Operations, Infinity Pharmaceuticals; Diane Nedelkoff, Director, Clinical and Investigator Portal Solutions, InnovoCommerce; Steve Stowers, Business Capability Management, R&D Global Development Informatics, Bristol-Myers Squibb; and Mark Vermette, Senior Director, Global IT CTMS, Quintiles on a panel discussing risk-based validation, 21 CFR Part 11 compliance, two-way discussion boards and implementation versus installation.
Other opportune sessions include:
Sponsors and Exhibitors include: ePharma Solutions, Pharmica Consulting, TCN e-Systems, innovocommerce, INTRALINKS, FireCrest Clinical, NextDocs, Compass IRB and Blue Sky Broadcast.
For more information on this event, please visit http://www.cbinet.com/Portals or call 800-817-8601. If you would like to apply for a press pass, please contact Lauren Donoghue at email@example.com or 339-298-2262.
A subsidiary of Advanstar Communications, CBI Research, Inc. offers Pharmaceutical and Healthcare conferences that serve senior executives and government officials by providing a unique platform for highly focused content and ideal networking opportunities with senior policy- and decision-makers. CBI events provide you with concrete, real-life examples that you can begin to apply at your organization immediately for significant impact on costs and revenue. For more information, please visit http://www.cbinet.com.
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-- Selecting the Development Route for a Clinical Trial Investigator Portal (Dory Rodriguez, MBA, Clinical Systems Lead, Takeda Global Research and Development, Inc. and Bill Dornback, B.S., Clinical Systems Lead, Takeda Global Research and Development, Inc.)
SOURCE Center for Business Intelligence
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