Driven by a Mission to Transform Healthcare

We have been in the trenches. On the audit hot seat. Accused of stifling innovation. Overwhelmed with the (growing!) number of regulatory requirements to monitor and manage. We hate the feeling of not knowing if I am missing a requirement, not knowing if I put an overly burdensome process in place and not knowing if our company is truly following our processes as much as you do.

Adam Foresman went into life science to help patients and clinicians by designing and manufacturing the latest technology at the highest quality. All of us and our family members deserve it! It is very challenging managing hundreds of regulatory requirements across 1000s of pages & conducting audits against them. We went into this industry to engineer products, lead clinical trials, do statistics & data science, and gather feedback talking to real people… Not this. This is why he formed Ryden. To save time and cost while gaining valuable insights that can only be achieved through continuous gap analyses and audits.

The entire Ryden team has been in well over 300+ audits of all different requirements. We have countless premarket submissions and QMS process implementations across all types of technologies. We have written industry standards, regulatory certification exam questions and given back to the quality and compliance community. Lastly we know how to implement AI in GXP environments having obtained multiple AI-enabled medical device clearances and been Information Security Officers protecting millions of patient medical records. We designed Ryden for all of us!