FAQ Friday with Amé Huige: answers to your questions regarding UK registration for custom-made devices

Daniëlle Motta "Our global registration team operates worldwide with market access. Together we determine your global regulatory strategy and the efficient roadmap to meet compliance to the local requirements, getting products registered and keeping your technical documentation up to date."

We are very excited about the many FAQ Friday questions we have received in the past months. Hopefully, you appreciate our expert vlogs and the answers were helpful.

🔎 In this weeks vlog Amé answers the question: As a custom device, our product is not labeled with a CE mark but has our EU Rep on the product label. Do we still have until June 20, 2023 to have a UK mark added to the label? Is there anything to be aware of for custom medical devices and sales into UK post Brexit?


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