ISO 13485 Certification: Ensuring Quality in Medical Devices

Fri, 21 Mar 2025 05:21:01 +0000

ISO 13485 is the internationally recognized standard for quality management systems (QMS) in the medical device industry. It provides a structured approach to ensure regulatory compliance, risk management, and product safety. Companies involved in the design, production, installation, and servicing of medical devices benefit from this certification by improving product quality and meeting global market requirements.