The Central Drugs Standard Control Organisation (CDSCO), under the Directorate General of Health Services in India, plays an important role in ensuring the safety, efficacy, and quality of drugs, cosmetics, and medical devices in the Indian market. Addressing the challenges posed by substandard and copyright products, the CDSCO has established comp
Preparing a Device Master File (DMF) as per the Medical Device Rules, 2017: A Guide by Morulaa HealthTech
Morulaa HealthTech, as the leading consultant in India for medical devices, simplifies the preparation of the Device Master File (DMF) in compliance with the Medical Device Rules and regulation (India MDR, 2017). Acting as your authorized agent in India, Morulaa ensures the DMF meets the regulatory requirements of the CDSCO medical device g