Working Sets: Working with existing Working Sets
Introduction to ISO 13485 Quality Management System for Medical Devices | Webinar recording
Watch this webinar recording with Danish Mairaj, Resyca’s Development Engineer. Danish has 10+ years of medical device design and development experience with a strong background in MedTech regulatory compliance and quality management. ISO 13485 is a crucially important standard for MedTech developers as it contains key requirements on Quality Management Systems for medical devices. In…