21. september 2016
Going From Manual to Automated Development Processes
Three Steps to an FDA and ISO Compliant Implementation
Has your company considered moving to a more efficient electronic product development process to manage BOMs, ECOs, Documents and Quality data but hesitated because of concerns about meeting compliance or weren’t quite sure where to begin or what to do?
Attend this webinar to learn from a medical device client, Autonomic Technologies, Inc. (ATI), a medical device company focused on developing innovative therapies for the treatment of severe headache, on why and how they transitioned from a paper-based system to an electronic Product Lifecycle Management (PLM) system.
Thursday the 22nd of September 2016
Time: 19:00 – 19:45 hr