Standards in Support of the EU Medical Devices Regulations

• 22/05/2023

The use of harmonised standards in support of the Medical Devices Regulations (MDR & IVDR) is a proven and trusted way to ensure compliance, quality, safety and efficiency of products, production processes, management systems, services and test-methods. They are developed as per the EU request to the European Standardisation Organisations (CEN & CENELEC) and cited in the Official Journal of the...