Thaneshwar Verma

Thaneshwar Verma is a seasoned professional in clinical research and drug safety with extensive experience in authoring critical regulatory documents such as Clinical Evaluation Plans (CEPs) and Clinical Evaluation Reports (CERs), primarily at Alcon, where responsibilities include ensuring compliance with EU MDR and MEDDEV regulations. Previous roles include serving as a Senior Drug Safety Associate at Qinecsa Solutions, handling vaccine safety data entry and adverse event evaluations, and as a Drug Safety Associate at PAREXEL, managing Individual Case Safety Reports (ICSRs) and ensuring adherence to international drug safety regulations. Thaneshwar's career began as a Senior Researcher at GD Research Center Pvt. Ltd., focusing on clinical trial data management and secondary research. Educational qualifications include a Master of Pharmacy in Pharmacology from Manipal Academy of Higher Education and a Bachelor of Pharmacy from Punjabi University.