PTC Integrity can help your organization ensure compliance with the recent FDA MDDS ruling (Medical Device Data Systems) which reclassifies medical device data systems as Class I devices and are subject to general regulatory control.
PTC Integrity can help your organization ensure compliance with the recent FDA MDDS ruling (Medical Device Data Systems) which reclassifies medical device data systems as Class I devices and are subject to general regulatory control.
Integrity provides a Quality Management system uniting stakeholders onto a common platform to provide automation and common processes across the development lifecycle, while other groups can be provided the Integrity Medical Device Solution with “out of the box” artifacts to support FDA Class I requirements.
Integrity manages all software system development processes and connects all software engineering artifacts, including requirements, models, code, and test, ensuring comprehensive lifecycle traceability. Integrity's open architecture integrates disparate tools into a streamlined software system engineering process, allowing coordination of software change and collaboration across the technology supply chain.
With Integrity, development teams improve productivity and quality, streamline compliance and gain complete product visibility, ultimately driving more innovative products into the market.