The deadline, 26 May 2021, for EU MDR is fast approaching.
The Danish Medicines Agency (Lægemiddelstyrelsen) recently published guidance regarding the new regulations and their consequences for both industry and Danish authorities. Read their guidance here (Danish only).
Keep abreast of the latest news and information regarding MDR and make sure your products are ready for the new regulations. SAXOCON can help you to ensure your products are qualified.
Are you ready? We are.
Check out how we can help here.