Sunfox Technologies Private Limited

1. Oversee the development, maintenance, and accuracy of technical documentation for medical devices. 2. Monitor and ensure compliance with post-market surveillance obligations as outlined in Article 10(10) of the EU MDR. 3. Serve as the primary point of contact for regulatory agencies regarding compliance matters related to EU MDR. 4. Collaborate with the Quality Assurance team to integrate regulatory compliance requirements into the organization's QMS.