gandharva marne

At PharmaEdge, I trained in drug safety monitoring and adverse event reporting. I learned about regulatory frameworks including ICH-GCP, WHO guidelines, and FDA/EMA requirements.

I also developed an understanding of risk management and pharmacovigilance workflows, including ICSR case processing, safety database workflows, and regulatory requirements.

During my internship at T. Walkers Pharmaceuticals Pvt. Ltd., I completed training in Quality Control and Production operations. I gained exposure to pharmaceutical manufacturing workflows, Quality Control procedures, and GMP compliance, documentation, and safety standards.

I’m seeking an entry-level opportunity to build a career in Pharmacovigilance and Drug Safety. My knowledge includes adverse event assessment, seriousness and causality assessment, MedDRA coding, case narrative writing, follow-up, safety data evaluation, and post-marketing surveillance.