A complete quality management system (QMS) includes solutions for CAPA, Deviations, Complaint Management and more, all operating as components of an integrated, closed-loop system. This is exactly what you will see during this one-hour online session.
Managing quality processes in accordance with 21 CFR Part 11 and related regulatory requirements involve collecting and documenting critical activities and incidents, and ensuring that appropriate notifications and actions follow.
During this session you will see a solution based on SharePoint 2010 including the ability to collect the required documentation, manage it in a compliant manner, notify the correct individuals and launch the required corrective or preventative processes. The result is an integrated, closed loop quality management system.
This one-hour session will cover:
An overview of SharePoint 2010 in the context of managing quality processes in a life sciences environment
A demonstration of a complete Deviation >> CAPA cycle, including initial documentation, notifications to the correct parties and generation of a resulting corrective action.
A discussion of how SharePoint 2010 addresses regulatory requirements for managing quality processes
For More information and Register to the webinar please use the below mentioned weblink: NextDocs Quality Management System - COMPLIMENTARY WEBINAR
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