If you are a manufacturer, importer, or distributor looking to test a medical device in India before commercial launch, you must obtain a Test License under the Medical Device Rules (MDR), 2017. The Test License is a mandatory approval issued by the Central Drugs Standard Control Organization (CDSCO) that allows you to import or manufacture devices solely for testing, evaluation, or c... https://www.corpseed.com/knowledge-centre/test-license-for-medical-devices-in-india-form-md-16-md-17