Transitioning from paper-based document control and change management to an electronic system can be a bit intimidating, particularly for regulated medical device companies. This webinar is hosted by Omnify Software with a client guest speaker sharing real world scenarios. Attendees will learn about why and how a medical device manufacturer should automate development processes with Product Lifecycle Management (PLM), things to be aware of, and three steps to a compliant implementation.
WHAT: Complimentary, educational webinar focused on the value of moving from paper processes to an electronic system to manage product information and how to do it compliantly.
WHEN: Thursday, August 4, 2016 at 1:00 P.M. eastern
WHERE: Event will be presented online; those interested in attending can register here.
WHO: Joseph Ko, Director of Quality for Autonomic Technologies (ATI), will share his experience configuring and implementing many computerized systems including Agile PLM, Expandable MRP, and Omnify Empower PLM. David Whitney, VP of Strategic Sales for Omnify Software will moderate the webinar.
We use cookies to help provide you with the best possible online experience.
By using this site, you agree that we may store and access cookies on your device.
You can find out more and set your own preferences here.
