Webinar - Online
This webinar addresses the obligations of sponsors, monitors, and investigators who conduct and verify clinical research that is governed by US FDA regulations and ICH guidelines.Monitoring systems should include specific components to ensure control of investigational product, data integrity, oversight of vendors, as well as other areas. The components of a quality monitoring system will be presented so that participants can assess their current practices for identifying gaps and risks, particularly in relation to preparing for regulatory inspections.
Speaker: Charles H Pierce
Organization: Global Compliance Trainings
For more information, please visit: http://www.globalcompliancetrainings.com/index.php?route=product/product&product_id=16&list=Charles%20H%20Pierce
30 May 2014 (10:00 AM - 01:00 PM)
201,N Squirrel road, Suite 1007, Auburn Hills, Michigan United States - 48326
Contact: John Gordan (webinar@globalcompliancetrainings.com)
Phone: 2482120588
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