About Me
I am a Bachelor in Pharmacy, with total experience of 13.5+ years bifurcated into[removed]Years in Pharmacovigilance and 11 + years as Clinical SAS Programmer. I am well verse with all the submission level expertise on CSR, BLA and DMC reporting guidelines for Dose Accelerated Studies, Vaccine, Diabetes, and Rare disease therapeutic extended over open labelled, blinded, double blinded, cross over and parallel studies.
Looking forward on this platform to extend the support for multiple stakeholders at a mutually agreed available time.
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