What is my role on the market? What are my duties as a manufacturer according to the Medical Devices Regulation (MDR)? BEO BERLIN can train you and your staff on this.
Standard in Focus: DIN EN ISO 10993-18
German version of EN ISO 10993-18:2020 Biological evaluation of medical devices – Part 18: Chemical characterisation of materials was published this month and replaces the version from 2009.
