Medical Device Vigilance: Important Considerations to Comply With the EU MDR
Vigilance reporting and postmarket surveillance of medical devices are among the many requirements documented in the EU MDR (2017/745) to ensure the...
Veranex Design Control Guide
Effectively managing all design control requirements can be a smooth process, if planned and implemented in line with the product, business goals and regulations to avoid challenges for medical device manufacturers.
To assist you with this endeavor, our team has meticulously mapped out key steps of the Design Control process.
Please submit the form to access the guide: