Srilekha Deka, PhD
Senior Vice President, Regulatory Affairs
Dr. Srilekha Deka is a seasoned biotechnology professional with extensive experience in commercializing molecular diagnostic assays. A proactive leader, she excels in managing projects from initiation to completion, particularly in the development of infectious disease assays across various qPCR platforms.
Her expertise includes project management, regulatory submissions, and the commercialization of IVD products, emphasizing process optimization and cost reduction. Known for her strong communication and team-building skills, Dr. Deka is dedicated to driving innovation in biotechnology.