FALLS CHURCH, Va. (PRWEB)
April 21, 2020
Transforming Quality Management with a Modern Cloud Solution
A Free FDAnews Webinar, Sponsored by Axendia and Veeva Systems
Tuesday, May 5, 2020 • 1:30 p.m. – 2:30 p.m. EDT
http://info.fdanews.com/transforming-quality-management
Is one’s quality management system (QMS) designed to create visibility, traceability and accountability?
Modernizing the processes will connect systems, processes and people to provide a foundation for quality transformation.
In this Axendia-sponsored webinar — Joe Vigil, director of quality management systems at Ultragenyx — Sandra K. Rodriguez, market analyst at Axendia and — Mike Jovanis, vice president quality at Veeva Systems — will discuss how a modern, cloud quality system can transform and simplify ones business procedures, drive quality improvement and improve collaboration with external partners.
Gain insights into:
•Why all clouds are not created equal
•How to evaluate a cloud solution in a regulated environment
•The pros and cons in evaluating a cloud solution
•The benefits of a modern cloud QMS
•Becoming cloud comfortable in a regulated environment
Reap the benefits of cloud technology and ensure compliance and improve quality by centralizing and integrating the quality processes.
Webinar Details:
Transforming Quality Management with a Modern Cloud Solution
A Free FDAnews Webinar, Sponsored by Axendia and Veeva Systems
Tuesday, May 5, 2020 • 1:30 p.m. – 2:30 p.m. EDT
http://info.fdanews.com/transforming-quality-management
Easy Ways to Register:
Online: http://info.fdanews.com/transforming-quality-management
By phone: 888.838.5578 or 703.538.7600
About FDAnews:
FDAnews is the premier provider of domestic and international regulatory, legislative, and business news and information for executives in industries regulated by the US FDA and the European Medicines Agency. Pharmaceutical and medical device professionals rely on FDAnews’ print and electronic newsletters, books and conferences to stay in compliance with international standards and the FDA’s complex and ever-changing regulations
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