It is well known in the medical device industry that the success of a company is driven by its ability to bring innovative, cost-effective, and compliant products to market quickly. And, in today’s global medical device market, proactive strategies are needed to ensure compliance with the regulatory requirements in global markets. As the Food and Drug Administration (FDA) and other regulatory bodies have embraced the concept of total product life cycle (TPLC) management, it has become the gold standard for guiding a medical device from concept to completion.
Device manufacturers need solutions that not only archive and manage data, but also facilitate the sharing of product and process data within the company, as well as with suppliers and partners. Learn more about how a Cloud PLM can provide an efficient, centralized system for managing design control, document control and change control processes.