Regulators in most medical device markets require registration to comply with post-market surveillance (PMS) obligations to maintain compliance. However, PMS rules can vary between different medical device markets, requiring manufacturers to develop customized approaches rather than one-size-fits-all.
With extensive experience in post-market surveillance requirements, the Riyadh Muttawra Medical team is equipped to act as your compliance partner long after your device hits the market. We can help you design and implement a PMS system that meets requirements in multiple markets and navigates regulatory challenges throughout the device lifecycle.
We can help determine when incidents can be reported and ensure surveillance reports are completed on time and in accordance with local requirements.
