Further, it is also indicated by the government that the applicant needs to ensure physical destruction of all un-exported quantity of drugs. This should be included as a condition of manufacturing license issued to the applicant by the state licensing authority. In the event of the cancellation ...
As per the new Rules, state licensing authority (SLA) has to send applications to the notified bodies appointed by the Central government for inspections and auditing of Class A and Class B category medical devices for compliance. Class C and Class D categories are audited by the CDSCO. As p...
Further, the applicant, in case has submitted an incomplete application on or before April 18, 2021, is required to ensure submission of all the necessary documents to the concerned authority by March 31, 2022. “Central Licensing Authority or State Licensing Authority, as the case may be, sha...