Biography

Ripal Gharia has completed her M.B.B.S. and M.D. in Pharmacology from Maharaja Krishnakumarsinhji Bhavnagar University – Gujarat and Post Graduate Diploma in Pharmacovigilance from Cliniminds, India. She is certified Project Management Professional (PMP) from prestigious Project Management Institute (PMI), USA. She has about 14+ years of working experience in clinical research in key roles as medical, regulatory and safety expert for various regulatory submissions such as FDA, EMA and DCGI in all therapeutic areas predominantly oncology and biosimilars. She has a close rapport with KOLs and subject experts in various therapeutic areas. Till now she has been part of more than 70+ studies in different phases of drug development. She possesses good communication & leadership skills, extensive monitoring experience, sound knowledge of clinical research & global regulatory requirements.

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Research Interest

Currently, at COD, she is involved in Strategy planning for the overall growth of the organization, plays a key role in establishing medical and scientific writing services, pharmacovigilance and regulatory affairs services, developing whitepapers/articles for publication in reputed journals/publications, actively seeks opportunities to represent the organization at national and international forums.