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.
GCP/ICH Obligations of Sponsors, Monitors, and Investigators: How to guarantee a clean inspection/audit
30 May 2014, michigan., United States
Introduction
Venue
201,N Squirrel road,, Auburn Hills,, Suite 1007,, michigan., 48326., United States
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Organised by
Global Compliance Trainings
Contact information
Mr john gordan
201,N Squirrel road,, Suite 1007,, Auburn Hills,, michigan., 48326., United States of America
2482120588
Contact us by email
201,N Squirrel road,, Suite 1007,, Auburn Hills,, michigan., 48326., United States of America
2482120588
Contact us by email
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