Tejas Aware's Linkedin Analytics

Since September 2023, I've had the opportunity to contribute to various projects focused on medical devices compliance with the European Medical Device Regulation (EU-MDR). Throughout these experiences, I've aimed to adapt to evolving regulatory requirements, paying meticulous attention to detail, and actively engaging in collaborative efforts with cross-functional teams. I've also pursued continuous learning to stay informed about industry changes and contribute to the success of regulatory initiatives. My responsibilities as Jr. executive are as follows: • Technical file gap assessment as per EU-MDR • Designing and review various labels as well as labelling plan. • Clinical Evaluation Documentation • Preparation of TCF as per EU-MDR • Clinical Evaluation