Abstract

Establishing a Nuclear Medicine Facility (NMF) in India involves navigating a complex regulatory landscape, primarily governed by the Atomic Energy Regulatory Board (AERB). This paper provides a detailed roadmap for setting up an NMF, covering critical aspects such as site plan approval, staffing requirements, procurement of equipment and radioactive sources, pre-commissioning inspections, and operational licensing. Emphasis is placed on adherence to safety standards, regulatory compliance, and the importance of periodic quality assurance and annual safety reporting. By following this structured approach, stakeholders can ensure the safe and efficient operation of nuclear medicine facilities, contributing to advancements in diagnostic and therapeutic healthcare in India.