Regulatory Affairs Specialist, having 1 year of experience in developing and compiling CMC related documents for submission to various drug regulatory authorities ensuring compliance of operations with governing regulatory agencies and compiling and reviewing Analytical Development Reports (ADR鈥檚) and Stability Study Reports (SSR鈥檚).
Additionally worked as, Analytical scientist and Patent analyst with 4.5 years of experience in both analytical as well as bio analytical departments in method development & stability analysis for solid oral dosage form. Experience in method development, method validation and study sample analysis by using LC MS/MS and spectra max to carry out BA/BE & Clinic...
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