Bio

Research Scholar from the National Institute of Pharmaceutical Education and Research (NIPER) and a consummate regulatory data professional with a proactive & and optimistic approach to help the pharmaceutical industry provide faster marketing approval and post-approval product optimization worldwide. A subject matter expert with more than 8 years of all-around experience in pharmaceuticals covering domain knowledge, regulatory processes, data, and technology. Experience in leading Digital/Data Initiatives, Regulatory Affairs, and project management at pharmaceutical companies. Certified Data Management Professional (CDMP®), Regulatory Affairs Certificate (RAC) and Project Management Professional (PMP®) with sound drug research and development to take ownership and handle multiple tasks. Ability to lead, innovate and contribute towards global projects working with cross-functional teams.