Clifton MedTech Consulting (Bristol UK) was founded in 2015 by Dr Lixia Zhou.

Clifton MedTech Consulting specializes in the regulatory approval process including CE marking, risk assessment and post market surveillance. Clifton MedTech Consulting addresses every aspect of the product approval process: software, electronics, mechanical, quality, and compliance. Our goal is to make sure you get the CE Marking you need to bring your device to market.

We love our customers and welcome your feedback and suggestions. Use our Contact Us page to tell us what we’re doing right or what we can improve on.