Ashwini Ghatpande

Ashwini has over 14 years of pharmaceutical industry experience in writing and editing clinical and regulatory documents and 10 years of diverse scientific research experience from academic institutions and pharmaceutical industry.

Prior to joining Biohaven, Ashwini worked at Bristol-Myers Squibb as a group director , where she led a team of writers to develop and implement regulatory documentation and product labeling strategy across therapeutic areas to support and facilitate global submissions and approvals. Ashwini’s medical writing expertise spans a wide variety of regulatory documents that are part of both US and international dossiers. In her previous role, she was part of a cross functional leadership team that implemented change management initiatives to improve cycle time and quality of regulatory documentation for global submissions. She brings extensive experience in resource planning, management and staff development to establish strategic, scientific, and technical expertise in support and delivery of high-quality regulatory documents. Ashwini earned her Masters and M.Phil in Molecular and Developmental Biology from the University of Pune, India.