Ishan Razdan

Ishan Razdan is currently a Global Medical Quality Expert at Sanofi, where they apply their extensive knowledge of regulatory guidelines and TMF processes to ensure compliance and quality in clinical research. They previously served as a QA Documentation Specialist at Kite Pharma and a TMF Specialist at Shionogi Inc., contributing to multiple phases of clinical studies. Ishan holds a Master’s degree in Regulatory Affairs for Drugs, Biologics, & Medical Devices from Northeastern University and a Bachelor of Technology in Biotechnology from Thapar Institute of Engineering & Technology. They have experience in global regulatory strategy and clinical protocol development through various academic projects and internships.