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 order to be able to build safe and high-quality medical technology products, you need to understand this regulation in-depth. Watch this webinar recording to find out if the standard applies to your organizations, what requirements ISO 13485 contains, and how it affects developers of medical technology. Watch now to better understand the purpose and benefits of ISO 13485!