Work smarter with the only platform designed by regulatory experts to manage your compliance process
BSI’s Compliance Navigator is the smart, simple way to manage your regulatory information for Medical Device and In Vitro Diagnostic products with UK, EU and MDSAP requirements. Stay ahead of regulatory updates, reduce adoption gaps, and accelerate market access through easy interpretation and implementation of high level standards and regulations.
Accelerate market access
- A true enterprise regulatory document and standards solution.
- Access thousands of standards and regulations, any place, any time.
- Anticipate changes with advance notifications of changes to standards.
- See exactly what's changed with our red lining tracked changes feature.
- Interpret regulatory rules and standards confidently with expert commentary and guidance.
It's time to say goodbye to stressful compliance
We fully understand the difficulty in remaining compliant in what is an ever-evolving regulatory landscape. BSI are committed to mitigating the regulatory challenges faced by medical device manufacturers. BSI Compliance Navigator holds over 7,000 documents essential for medical device compliance, in multiple jurisdictions across the world. From tackling the MDR transition, to applying for 510(k) clearance or PMA, Compliance Navigator is your partner in managing medical devices regulation and standards management. With unlimited user access available, there's no better time to try. Request a free trial today via the form to see how we can help!
