Streamline Quality Metrics Through Innovative Technology
Wednesday, May 11, 2016 • 1:30 p.m. – 2:30 p.m. EDT • An FDAnews FREE Webinar
Your Expert Presenters
Scott has worked at Sparta Systems for over 11 years with 13 years of Life Sciences Software Industry experience as well as Professional Services experience with dozens of Quality Management System implementations for Life Science customers. Scott holds a B.S. in Computer Science, Minor in Cognitive Science from Villanova University.
Joe is a senior member of the Sparta Systems sales team, leading up the Global Sales Operations team. Joe has a wealth of experience in enterprise solution value messaging and sales processes; and in important technology trends such as Big Data, Analytics and SaaS. Prior to joining Sparta Systems, Joe spent four years at a leading market research data, technology and consulting company, where he was instrumental in the build-out of a sales capability focused on the organization's advanced technology offerings. Joe holds a Bachelor of Engineering degree from the Colorado School of Mines.
Register for this FREE webinar below:
With FDA finalizing its quality metrics guidelines, manufacturers are eager to understand what its expectations will be. Once defined, companies need to ensure they are collecting those data points across all manufacturing sites and from multiple systems.
Criteria for technology solutions should include the ability to integrate with other key systems to collect required data, populate reports and electronic submissions to FDA. Your company will need to make significant changes to or adopt new processes, procedures, personnel and IT/IS tools.
Join us on May 11th for a FREE webinar that will show you how to use innovative technology to streamline your quality metrics initiative.
You will learn:
How metrics fit into the overall vision on quality programs
How to implement the required quality metrics with internal company data used to monitor quality systems
What tools are available to capture and measure quality information from manufacturing sites, CROs and suppliers
If you are looking to implement a reporting framework that produces reliable, useful data that meets the FDA requirements, register today.
Who Should Attend
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