Pijus Nandi

Accomplished Pharmacovigilance Professional with 6+ years of experience specializing in intake activities, end-to-end ICSR processing, adverse event assessment, MedDRA coding, and global regulatory submissions. Proven track record of handling safety data across clinical trials, post-marketing surveillance (PMS), and vaccines while ensuring strict compliance with SOPs and global regulations. Expert in navigating advanced safety databases, including Argus Safety, ARISg, LSMV, and Sapphire, as well as managing global submission portals.