the Medical Device Rules, 2016.Union territory Rules of Dadra and Nagar Haveli and Daman and Diu · 1940
(1) The Notified Body shall forward a detailed descriptive report giving findings on each aspect of audit along with recommendations after completion of audit in accordance with the provisions of rule 18, to the State Licensing Authority or Central Licensing Authority, as the case may be, through online portal of the Government referred in rule 15, with a copy to the manufacturer.
(2) The Medical Device Officer shall forward a detailed descriptive report giving findings on each aspect of inspection along with recommendations after completion of inspection in accordance with the provisions of rule 18, to the Central Licensing Authority, through online portal of the Central Government referred in rule 15, with a copy to the manufacturer.
Grant of licence to manufacture for sale and distribution of medical device.