Ganesh Chonde

Background

About Ganesh Chonde

I am a Master of Science postgraduate, in Pharmaceutical Regulatory Affairs from SETU Carlow and a Doctor of Pharmacy graduate with professional experience in Pharmacovigilance as an Operation Specialist for 3.9 years at IQVIA Asia Pacific. I have Extensive experience with PV operations and Compliance Management including end-to-end case processing activities such as Case intake, Book-in, Triage, Safety Database entry, Quality checks, Submissions, Coding relevant Adverse events, Concomitant and Suspect medications, Past medical history with MedDRA, Causality, and Listedness assessment, Writing descriptive narratives and Generating queries pertinent to Post- Marketing and Clinical trials (oncology) case reports. Also, to manage reporting/submission/distribution of safety reports/updates/information like SAE, SR, IN/SUSAR, PSUR, Biannual SUSAR Listing, DSUR to Local Health Authorities (LHA) and/or clinical operations in co-operation with other CPO Departments. Pharm D | Clinical Operations | Pharmacovigilance (Post Market Surveillance)| Regulatory Affairs | Regulatory Compliance | Clinical Trial | Literature | BOT RPA | Clinical and Pharmacological Expertise| RCA | CAPA | Compliance Handling and Maintenance