What are the legal challenges of bringing such innovative and scalable products to the market? In this webinar, we will explore a case study…
The UK’s Medicines and Healthcare products Regulatory Agency (MHRA) updated its guidance on medical device standalone software last month. We’ve set out our top 5 takeaways from the new guidance
Delay of MDR Implementation and its Implications for Brexit The recent postponement of the Medical Device Regulation 2017/745 (“MDR”) means its full application will…