Neha Keral

Dr. Neha Keral is an experienced regulatory professional specializing in clinical evaluation, PMS documentation, and medical writing for global regulatory compliance, including EU MDR, US FDA, TGA, MHRA, Health Canada, NMPA, and HSA. She collaborates with cross-functional teams to develop high-quality regulatory submissions across various therapeutic areas.

With a Ph.D. in Life Sciences focused on antimicrobial and anticancer research, Dr. Keral brings a scientific approach to regulatory strategy. At Celegence, she leads documentation processes, ensures compliance, mentors teams, and drives regulatory excellence in medical devices. Passionate about the intersection of science and medical innovation, she is dedicated to advancing regulatory solutions that impact healthcare.