12 years of experience (11 years of regulatory affairs experience for regulated/semi-regulated markets and 1 year of Analytical Research).
Worked with Ranbaxy Limited, Wockhardt Limited, Jubilant organosys, Sandoz pvt. limited etc.
Expertise: eCTD, NeeS, CTD, Country specific Dossier, Variation assessment, Regulatory compliance- Solid oral, Oral liquid, Injectable, ophthalmic, Cream, Ointments etc.
Country of Submission: US/EU (National Submission/DCP/MRP), Canada, GCC, MENA, Jordan, ASEAN, CIS, Tunisia, Turkey, Tanzania, Kenya, Uganda, South Africa, Brazil etc.
Ability to explore any new country requirements for product classification, submission, pricing, time for approval etc.
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