Self-driven Regulatory Affairs Associate with two years of experience in Medical device Regulatory affairs. I hold a Master's in Biomedical Regulatory affairs from the University of Washington, specializing in medical device regulations, clinical trials, and technical writing. Prior to this, I worked as a research fellow at CCMB, India. I am familiar with new product development and registration, product validation, regulatory strategy, and Regulatory filings for Class II medical devices in the US, EU, APAC, and LATAM regions. I am passionate about my field of study, I am constantly looking to expand my skills and learn from this field, which has a great deal to offer.