Medical device registrants are generally in which department

Drug supervision and management department. Medical device registrars are responsible for the registration and audit of medical devices, but also to undertake the management of medical device registrants, in the drug supervision and management department, is the most important regulatory department. Medical devices are instruments, equipment, apparatus, in vitro diagnostic reagents and calibrators, materials and other similar or related items used directly or indirectly in the human body, including the required computer software.