CEPK consult

Experts in CE, FDA and GDPR for Medicine, Medical Devices and Cosmetic Surgery devices

“I think it is very unfortunate if the regulatory processes, whether for CE marking or FDA, become a hindrance for highly innovate products.

I started CEPK because I want to help manufacturers reach the finish line and get their devices on the market, so we can save/improve human lives together.”

- Cecilia Tran-Jørgensen, Owner & Lead Auditor


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