Do you have a Class I device that will be up-classified under MDR EU 2017/745? Are you ready for 26th May 2024 deadline? The clock is ticking….
Solicitor, Alison Newstead, explains why compliance is crucial to the continued success of your business and how failings can lead to fines and even a prison sentence.
Small and medium-sized enterprises face complex and ever-changing medical device regulation, which can be a daunting challenge. However, with the help of a specialized consultancy team, you
Streamline Medical Device Regulatory Compliance with Advena Consultancy – Tailored Services for SMEs Navigating the complex regulatory landscape can be a daunting task for small and
