Prateek Bansal

WORK HISTORY

EDUCATION

ABOUT PRATEEK BANSAL

I am a Safety and PV coordinator in Pharmacovigilance with a strong focus on ensuring patient safety and regulatory compliance across the drug lifecycle. My work centers on case processing, safety reporting, and signal detection, helping transform raw safety data into meaningful insights that support safer medicines.I specialize in Individual Case Safety Reports (ICSRs), including case intake, medical review, MedDRA coding, narrative writing, and submission in compliance with ICH-GCP, ICH-E2B, and global regulatory requirements (FDA, EMA, MHRA). I work with both serious and non-serious adverse event reports, ensuring accuracy, timeliness, and high data quality.What I bring is reliability and attention to detail in a field where precision matters. I help teams reduce compliance risk, improve case quality, and maintain inspection readiness by following SOPs and quality standards consistently. I’m comfortable working in fast-paced environments, managing multiple cases, and collaborating with cross-functional teams in clinical research and safety operations.My goal is simple: protect patients, support regulators, and strengthen drug safety systems through high-quality pharmacovigilance work.Core Skills:Pharmacovigilance • Drug Safety • ICSR Processing • MedDRA Coding • Narrative Writing • SAE Reporting • Aggregate Reports • Signal Detection • Regulatory Compliance • Clinical Safety • Quality Review