An enthusiastic person with highly motivated and leadership skills having bachelors of engineering degree in Biomedical Engineering with total 6 years of experience in Regulatory Affairs & Medical coding Expertise in submissions for multiple medical devices and managed different compliance activities to (EU) MDR 2017/745 and IVDR, USFDA 510(K), 513 (g), 501(k), MDUFMA, and ISO standards among other international market authorizations of productsExpert in implementation of each step of project. Eager to learn new technologies and methodologies. Always willing to innovate the new things which can improve the existing technology