Simplifying IVDR Compliance for Your IVD Business Expanding your IVD business into the EU? Then you’ve met the IVDR, the regulatory beast reshaping how diagnostic devices are approved. It’s dense,…
Author: Cert 3 Global
Cert 3 Global delivers expert medical device regulatory consulting services to manufacturers worldwide. We guide clients through US FDA 510k consulting, FDA food supplement registration, and toy product registration services. With deep knowledge of EU, UK, and US regulations, we ensure full compliance across medical device, food & supply, and cosmetic & toy sectors.