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Arpana Prasad
Arpana Prasad oversees and directs quality systems for bioequivalence (BA/BE) studies, early-phase, and late-phase clinical trials at Cliantha Research. With over 27 years of extensive clinical research experience, she ensures compliance with global regulatory standards.
Before joining Cliantha Research, she spent 8 years at Ranbaxy Research Labs and has successfully managed 150+ regulatory inspections from major agencies, including USFDA, AGES, UKMHRA, WHO, ANSM, and DCGI. Her expertise spans clinical research processes, GCP, GLP, and international regulatory requirements.
She holds a Bachelor’s degree in Applied Sciences (Analytical Chemistry) and an MBA in Operations Management.