Solutions
Success Stories
About Us
Jobs
Select the person you want to talk to
Medical Device Regulation (MDR, International and Risk Class 1 to 3)
IVD, Clinical Affairs, Notified Bodies, Regulatory Strategy
Partnerships, Investor Relations & everything else
Software Validation, Cybersecurity/EU AI Act in MedTech
CertHub offers AI-fueled software solutions for Technical Documentation, QMS and Design Control - tailored to the MedTech industry.
© CertHub 2025