Manasa Survi is a Clinical Regulatory Affairs Manager at XVIVO with previous roles in regulatory affairs and clinical operations at Takeda and Phio Pharmaceuticals Corp. Manasa also has experience as a Research Ethics Guidelines INTERN at Harvard School of Public Health. Manasa has a Master's Degree in Regulatory Affairs for Drugs, Biologics, and Medical Devices from Northeastern University, and a Bachelor's Degree in Pharmacy/Pharmaceutical Sciences from Jawaharlal Nehru Technological University. Additionally, Manasa has completed a 140 Hour Clinical Research Associate Training Program in Medical Research Management.
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