I’m a clinically trained dentist with a passion for patient safety and evidence-based healthcare, now building my career in pharmacovigilance and clinical research. My background includes hands-on clinical experience, detailed case documentation, and a strong commitment to regulatory standards. I hold an Executive Program in Clinical Research (Distinction) and Good Clinical Practice certification from Apollo Research and Innovations, alongside advanced training in pharmacovigilance, ICH guidelines, and MedDRA coding. I’m especially interested in adverse event reporting, causality assessment, and signal detection, and how these processes translate into real-world improvements in drug safety. My goal is to combine clinical insight with regulatory expertise to help protect patients and support safer therapeutic outcomes worldwide. Vision: To contribute to global pharmacovigilance systems that make medicines safer for every patient, everywhere.