Pavankalyan Banavath
Regulatory Project Management @MSN Laboratories
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WORK HISTORY
Regulatory Project Management @MSN Laboratories
Hyderabad, IN
Coordinating regulatory documentation and dossier submissions across global markets.* Collaborating with cross-functional teams including R&D, QC,QA, IP, Legal, and Marketing.* Supporting analytical and shipment documentation, as well as regulatory communications with country teams.
EDUCATION
National Institute of Pharmaceutical Education and Research (NIPER)
M.S.Pharm , Regulatory Toxicology
Sri Indu Institutions
Bachelor's Degree, Pharmacy
Arabindo high school
Ssc
ABOUT PAVANKALYAN BANAVATH
I am a detail-oriented Regulatory Affairs professional with an M.S. Pharm in Regulatory Toxicology from NIPER-Hajipur. My expertise includes regulatory submissions (eCTD, CTD, IND, NDA, ANDA, DMF, MAA) and compliance with ICH, US FDA, GLP, and GCP guidelines.Skilled in SOP drafting, study protocol implementation, and bioanalytical techniques (IHC, ELISA, Western blotting), I also have research experience in energy metabolism in cranial-irradiated mice. Key Skills: Regulatory submissions, compliance, SOP drafting, behavioural assessments, MS Office, Any-maze Achievements: GPAT, NIPER qualified | ASPICON 2023 presenter | Certified in Drug Regulatory Affairs & Drug Development
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