CDSCO audit for medical device manufacturers is a regulatory inspection conducted to verify compliance with the Medical Device Rules (MDR). It ensures that manufacturers follow Good Manufacturing Practices (GMP) and maintain a robust Quality Management System (QMS)....
Central Drugs Standard Control Organization (CDSCO) regulates and controls all medical devices entering the Indian market. You have to mandatorily secure the CDSCO medical device registration to launch your product in India. In this blog, we have prepared a detailed...
Central Drugs Standard Control Organization (CDSCO) regulates and monitors all medical devices in India. The CDSCO MD9 license permits the manufacture of class C and D medical devices in India. Class C and D medical devices are strictly regulated owing to their risk...
The CDSCO regulates the import of medical devices into India. Hence, you have to mandatorily secure the CDSCO MD15 import license to import your medical devices into India. It is the gateway for importing and selling imported medical devices in India. In this...
CDSCO notice, dated May 4, 2026, stated that long-pending applications on the SUGAM portal awaiting query response will be rejected. It directs all applicants to respond to regulatory queries within 30 days of issuance. The notice highlights that numerous applications...