Complete Procedure to Meet the CDSCO License Mandate of Class C & D Non-Notified Medical Devices
Overview of the CDSCO License Mandate The Central Drugs Standard Control Organisation (CDSCO) is the regulatory body that manages medical device registration in India under the Ministry of Health & Family Welfare. The main aim of CDSCO is to ensure that medical devices are...
Read More
Blog
Medical devices in India are manufactured under the rules and regulations set by the regulatory authority of India, that is, CDSCO. In India, to manufacture a medical device, one should have a...
Blog
ISO 14385 Medical Devices Certification: Definition ISO 13485 Medical Devices certification, Medical Devices-quality management system (QMS) is an internationally agreed standard. It sets out the regulatory requirements for quality management systems specific...
Blog
India's central consumer protection body published rules for preventing misleading commercials and endorsements for misleading advertisements 2022 on June 9th, 2020. CCPA announced the Guidelines to fulfill the duties given to CCPA...
Blog
The new draft bill consists of a few new definitions such as clinical trials, over-the-counter drugs, manufacturers, cosmetics, medical devices, new drugs, bioavailability, investigational new drugs, imported spurious drugs, predicate devices and...
End-to-End Regulatory Solutions for Domestic and International Markets
ENQUIRE NOW
KNOW MORE, LEARN MORE, ENGAGE MORE.
“Video-Only” Resource For Ease Of Understanding
