Rakesh Barmy
inspections
pharmacovigilance and clinical research
Lambda Therapeutic Research
India
Biography
Mr Rakesh Barmy, M Pharm (Pharmacology) has more than 10 years of experience in the areas of pharmacovigilance and clinical research. He has excellent working knowledge of the EU/US legislation as well as local requirements in the ROW. He has been involved in various pharmacovigilance audits and has also gained exposure to EU and ROW authority inspections which has enhanced his understanding of regulatory requirements. Presently, he is working as EU-QPPV for various clients and is responsible for establishing and maintaining pharmacovigilance system at Lambda for various premier clients. He specializes in Pharmacovigilance Audits, Pharmacovigilance System strategic design, signal & risk management, Quality Management & SOP development, PV System Master File (PSMF) Development, etc.
Research Interest
pharmacovigilance and clinical research
