Clinical Trial Site Quality Management System
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Website http://www.onlinecompliancepanel.com/webinar/ClinicalTrials-501075/OCT-2015-ES |
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Category Quality Management Systems, Document Management Programs, Document Control, Training Programs, Audit programs- internal and external, CAPA Programs, Root cause Analysis
Deadline: October 28, 2015 | Date: October 29, 2015
Venue/Country: online Webinar, U.S.A
Updated: 2015-10-07 14:46:59 (GMT+9)
Call For Papers - CFP
Clinical Trial Site Quality Management SystemInstructor: Susan LeisterProduct ID: 501075Level: IntermediateObjectives of the PresentationDiscuss the key components of a QMSDiscuss the key elements of a document management programDiscuss the critical aspects of a training programDiscuss the key elements of an audit programDiscuss the key components of a CAPA programDiscuss the critical aspects of root cause analysisWhy Should you AttendAttending this session will help one gain additional quality skills and tools which can improve your overall site performance. This session will help a clinical site build a stronger Quality Management System by eliminating potential weaknesses within their quality programs. Having a well-organized and effective QMS helps the site be inspection ready for the various regulatory audits that may come their way. This webinar reviews the critical elements of the QMS and discuss challenges, best practices, and things to consider to help clinical staff develop or improve their system.Areas CoveredQuality Management SystemsDocument Management ProgramsDocument ControlTraining ProgramsAudit programs - internal and external, CAPA ProgramsRoot cause AnalysisChange ControlCustomer ComplaintWho can BenefitClinical Study StaffClinical Quality StaffMonitorsSponsorsFor Registration -http://www.onlinecompliancepanel.com/webinar/ClinicalTrials-501075/OCT-2015-ESNote : Use coupon code 1371 and get 10% off on Registration
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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