Pharmaceutical Regulatory Affairs

Biography

Rama K Pidaparti is a Ph.D candidate from ASU and attended Life Sciences and HealthCare courses from BEP Program at Sloan School of Management, MIT. Has over 20 years of industry experience and is currently Principal Consultant, Medical Devices vertical, Wipro Technologies. Rama worked at many large Global Medical Devices and Biotech drug companies as a consultant; GEHC, J&J, Genzyme, Genentec, Zimmer, and Boston Scientific to name a few. He is an advisory consultant helping clients with Business Processes and Validated implementations of Computerized Systems for R&D, Quality and Regulatory areas and also an invited speaker on Quality and Regulatory Compliance topics at Life Sciences events in the past 10 years.

Research Interest

SDLC, PLM, SCM, QMS (Complaints, CAPAs, Supplier Controls, Document and Change Management) & Regulatory Affairs, including Information Security and Risk Management