Armanbir Singh

Background

About Armanbir Singh

As a passionate Regulatory Affairs professional, I am dedicated to ensuring that life-saving products meet global standards of safety, quality, and efficacy. Currently pursuing my Master’s in Regulatory Affairs at Northeastern University, I am building a strong foundation in regulatory strategy, compliance, and product lifecycle management across pharmaceutical, biotech, and medical device industries. I have hands-on knowledge of FDA, Health Canada, and EMA regulations, as well as experience preparing regulatory submissions like INDs, CTAs, and NDAs. With a background in science and a keen eye for detail, I am committed to supporting organizations in navigating complex regulatory landscapes efficiently and ethically. I am excited to contribute my skills in regulatory writing, risk assessment, and cross-functional collaboration to innovative teams. Always eager to learn and grow, I aspire to make a meaningful impact in the world of healthcare and patient safety. Areas of Interest: Regulatory Strategy & Submissions Quality Compliance (GxP, ICH Guidelines) Clinical Trials & Product Development Risk Management & Labeling Compliance Global Regulatory Affairs Let’s connect!