Never be out of compliance again with “state-of-the-art” standards
Eliminate the administrative functions of regulatory affairs by not having to chase down documents when a standard changes.
Get notified of changing standards and know exactly what products and essential principles are affected.
Integrated with all other RIMSYS software solutions so you never miss another update again.
Search through our database of 100,000+ standards
Once you find the relevant standards, simply add them to “My Standards Library” where you can keep track of any changes
Link standards to your products to understand and build a comprehensive regulatory standards database specific to your products and company
If a standard changes, receive notification of those changes and the products that are impacted
into our other solutions
Track registrations, renewals, expirations, notes, tasks, important dates, regulatory documents, and collaborate with in-country sponsors.
The FIRST and ONLY software created for your products’ essential principles! Collaborate, link standards, apply evidence, and get notified when standards change.
Want to Know More?
RIMSYS Regulatory Management Software is a collaboration hub to help medical device companies actively navigate the changing regulatory landscape. RIMSYS offers a suite of cloud-based regulatory affairs software solutions for the medical device industry to manage global product registrations, standards, essential principles, regulatory documents, and more.
Medical Device Product Registrations
Medical Device Standards Management
Medical Device Essential Principles