With growing regulatory requirements in the medical device industry, manufacturers need to streamline their product-related processes to create a more sustainable way toward continuous compliance.
Context (and traceability) is king...as a medical device manufacturing engineer, we were forced to waste a lot of time. How did we solve the problem? With access to the Aras PLM Platform.
Many companies across the medical device industry still suffer from manual workflows in their Design Control processes. As a result, an increasing amount of flawed products are being recalled from the marketplace.
Document control is critical in medical device development and manufacturing. Unfortunately, many engineers are hampered by manual processes. In this post, I'll show you a better way to manage documentation.