Clinical Trial Site Quality Management System
About This Event
Clinical Trial Site Quality Management System
Instructor: Susan Leister
Product ID: 501075
Level: Intermediate
Description
Attend this webinar to understand the key components of a QMS, key elements of a document management program, critical aspects of a training program, more.
Objectives of the Presentation
Discuss the key components of a QMS
Discuss the key elements of a document management program
Discuss the critical aspects of a training program
Discuss the key elements of an audit program
Discuss the key components of a CAPA program
Discuss the critical aspects of root cause analysis
Why Should you Attend
Attending 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 Covered
Quality Management Systems
Document Management Programs
Document Control
Training Programs
Audit programs - internal and external, CAPA Programs
Root cause Analysis
Change Control
Customer Complaint
Who can Benefit
Clinical Study Staff
Clinical Quality Staff
Monitors
Sponsors
For Registration -
http://www.onlinecompliancepanel.com/webinar/ClinicalTrials-501075/OCT-2015-ES
Note : Use coupon code 1371 and get 10% off on Registration