Rashmi Dodia

Rashmi Dodia has a diverse background in regulatory affairs and business development. Rashmi is currently working as an Associate Director of Regulatory Affairs at Boston Pharmaceuticals, where they manage regulatory affairs activities. Prior to this, Rashmi worked at NeuMoDx Molecular Inc. as a Sr. Regulatory Affairs Specialist, where they established regulatory operations infrastructure and led the development of post-market surveillance activities. Rashmi also has experience in regulatory operations and technical management at MMS, where they published regulatory submissions and developed workflows for review cycles. Rashmi started their career as an intern at Johns Hopkins Technology Transfer and MMS Holdings Inc., gaining experience in technology transfer and regulatory operations. Additionally, they worked in business development at LifeCell international Pvt. Ltd. and volunteered in clinical research at Cipla Cancer Palliative Care Center. Overall, Rashmi has a strong background in regulatory affairs and a demonstrated ability to successfully manage regulatory operations.

Rashmi Dodia completed their Bachelor of Science (B.Sc) in Biomedical Sciences, General from the University of Central Lancashire from 2008 to 2011. Rashmi then pursued their Master of Science (MS) in Regulatory Science from The Johns Hopkins University between 2012 and 2014. In June 2018, they obtained a Regulatory Affairs Certification from the Regulatory Affairs Professionals Society (RAPS) in the US.