The Indian medical device industry is considered as one of the fastest growing. The Indian regulatory agency, the CDSCO, make a conscious effort to improve their regulatory regime to release safe and efficient medical devices into the market. The CDSCO under the MDR 2020, the recent amendment of Medical Device Rules (MDR) 2017, now requires all the devices imported and placed in Indian market to be mandatorily listed by October 2021 followed by their registration in upcoming years. As a device manufacturer, do you understand India’s current Regulatory dynamics, applicable regulations, and different device registration pathways? To help you better understand the vast Regulatory landscape of the Indian medical device industry, we bring you an exclusive webinar on " Indian Medical Device Regulatory Landscape- A Deep Dive" on 22nd September 2021.