Introduction Within the evolving framework of medical device regulations, the European Union Medical Device Regulation (MDR) 2017/745 places a significant […]
Introduction to MDR product compliance as a distributor For medical device distributors operating within the European Union, ensuring the compliance
Introduction The European Union Medical Device Regulation (MDR) 2017/745 introduces the significant role of the Person Responsible for Regulatory Compliance
Introduction to MDR distributor obligations The European Union Medical Device Regulation (MDR) 2017/745 has significantly reshaped the landscape for all
Distributors serve as a critical link in the medical device supply chain, connecting manufacturers with end users such as hospitals,
