Medical Device Certification
Medical devices play a crucial role in healthcare, directly influencing patients’ health, safety and well-being. Medical device manufacturers operate within a highly regulated environment in which product safety and performance, effective quality management and regulatory compliance are essential throughout the device lifecycle.
Bureau Veritas supports medical device manufacturers through a comprehensive range of certification services, including conformity assessment under Regulation (EU) 2017/745 (MDR) and Quality Management System certification according to ISO 13485.
Through our dedicated team in Switzerland, manufacturers benefit from a local point of contact, multilingual communication and access to Bureau Veritas’ international network of qualified medical device experts.
Bureau Veritas provides a comprehensive range of certification and conformity assessment services for medical devices, supporting manufacturers in demonstrating compliance with applicable quality, safety and regulatory requirements.
