Accelerating Medical Device Innovation While Mastering the FDA Case for Quality – The Vital Role of PLM
We live in an age where innovation is driven by Digital Transformation. Medical Device Companies are facing the unique challenge of remaining competitive in an environment where increasing regulatory complexity is coupled with the demand for lower cost medical innovations in a connected world.
Intense analysis of device quality data and feedback, from regulatory and industry stakeholders led the FDA to establish the Case for Quality. The objective being the advancement of medical device quality and safety to achieve better patient outcomes. The Case for Quality elevates the focus of medical device stakeholders from baseline regulatory compliance to sustained, predictive practices. This will inevitably lead to changes in procedures for product design and development.
How can Medical Device Companies master the FDA Case for Quality in a time when Digital Transformation of the industry leads to increasingly complex, connected and data driven products and services?
PTC invites you to join other leaders and industry experts in an interactive environment aimed at facilitating discussion, networking and the sharing of ideas and best practices. Together we explore how Product Lifecycle Management (PLM) can play a vital role in bringing Medical Devices to market faster, reducing product development costs and accelerating innovation in a highly-regulated environment.
At this event you will be able to:
Understand how the leading industry initiatives by the FDA and the European Commission impact the product lifecycle of your products.
Learn how other companies addressed associated challenges and opportunities within their organizations through PLM.
Discuss how PLM can create the foundation for Digital Transformation of Medical Device Manufacturers.
Network with peers who are transforming their own organizations and processes to get ahead and stay ahead.
Be part of the newly formed PTC Medical Device Customer Community.