Medical Devices and IVDs
Establish, audit or remediate your quality systems with guidance from our team of former regulators. Our experts help you prepare for market, mitigate risk and achieve sustainable compliance with country-specific regulations and international standards.
How Can We Help?
Two of the Most Common IVDR Challenges (With Solutions)
An Easier Approach to IVDR Technical Documentation
ISO 10993-23: The "Step-Wise" Approach to Evaluate Potential Irritants in Medical Devices Becomes Effective
News and Events
The State of Pharma Quality, GMP Certificates, November Pharma News Update
November 1, 2021
Meet NSF at Making Pharma 2021
August 31, 2021
Are You a Medical Device and IVD Expert? Join Our Consulting Team!
August 9, 2021
NSF Launches New IVD App
January 18, 2021