Meet Our Instructors
Susmita Sahu

Ms Sahu has supported multiple new drug approval submissions for critical diseases to global health authorities such as FDA (US) and EMA (EU). Her regulatory document expertize includes writing clinical study reports, protocols, informed consent forms, clinical efficacy and safety summaries, non-clinical summaries, and investigator brochures. Her key responsibilities at MMS include diverse work force management, providing technical guidance to the team, and training writers on various regulatory documents. She enjoys mentoring new medical writers and has developed many document specific training exercises.”