Krutika is a director of our digital evidence generation practice within ZS’s digital connected health group.
Working for the healthcare and digital medicine industries, Krutika has led the development and regulation of medical devices across B2B and B2B2C enterprise software and mobile apps. She has hands-on experience supporting quality, compliance, efficiency and safety throughout the digital health product lifecycle for diverse areas of healthcare payers and providers.
Prior to joining ZS, Krutika led digital medicine and regulation teams for a healthcare company, where she gathered and submitted clinical validation and regulatory approvals for medical devices with AI-powered digital care navigation, therapeutics and virtual care solutions. She has led a clinical and research group for conducting human factors studies and patient-centric studies, including medical device interventions, drug compatibility and longitudinal cohorts, as part of the German Research Foundation and the Federal Ministry of Education and Research to build innovative health tech solutions.
Krutika has a Ph.D. in neurophysiology from Technische Universität Dresden and an M.S. in human factors from the University of Idaho.