Many companies look at their quality and compliance programs as obligations or burdens. However, connecting quality and compliance processes is all about business performance, and having the ability to execute and accelerate the business, while reducing risk, improving quality and meeting all regulatory demands.
Connecting quality and compliance processes and the ensuing productivity gain is an opportunity that all regulated companies should recognize.
A comprehensive unified Quality Solution contains capabilities ranging from Document Control through Quality Processes and Learning Management, accessed through one centralized interface.
In this webinar, our quality expert will discuss the core components of a new comprehensive approach to Quality and how it can deliver business efficiencies as well as effortless regulatory compliance.
Key Learning objectives:
- What are the key essentials of an effective Quality Management System?
- FDA Regulated eDMS, utilizing DIA ICH guidelines
- How to establish best practice SOP, Deviation, CAPA, Change Controls, Complaint and Audit processes including event handling
- Demonstration of comprehensive Quality capability in a unified environment showcasing an integrated eDMS, QMS and LMS
Cyril Walsh, Sr. Solutions Consultant, Dassault Systèmes BIOVIA
Date: November 30, 2017
Time: 3:00pm (GMT)/ 10:00am (EDT)
Please complete this form to register to reserve your seat at this webinar»