Ayush Tomar

As a Regulatory Officer, I have extensive experience in the registration of medical devices, ensuring that all necessary documentation complies with regulatory standards. I am responsible for preparing and submitting critical applications for import/manufacturing licenses and creating detailed Device Master Files to support the regulatory process. I also manage complaint handling and ensure the timely resolution of any issues that arise. In my role, I frequently interact with the Central Drugs Standard Control Organization (CDSCO), coordinating visits and responding to queries related to regulatory compliance. My focus is on analysing these queries and providing clear, accurate replies to ensure smooth operations and compliance. With a solid understanding of the regulatory landscape, I am dedicated to supporting the safe and efficient market entry of medical devices, navigating complex requirements while maintaining the highest safety and compliance standards.