Expertise in Pharmaceutical Secondary Research, Data Analysis, Clinical Trials, and Regulatory Affairs. 11+ years of experience in drug competitive intelligence & Strategic decision support, Portfolio Management with expertise in Regulated (US, EU, Japan) and Emerging markets portfolios for generic and branded generic markets. Regulatory Milestones, Contract Manufacturing knowledge. Handled IMS, Newport, Medtrack, Citeline, Alphasense, GlobalData, PharmSource databases.