Class C & D Medical Devices
It is now prominent that in order to maintain market access starting on š¢š°šš¼šÆš²šæ š, š®š¬š®šÆ all Class C and D medical devices must obtain a #license (Manufacturing/Import). According to GSR 102 (E) dated February 11, 2020, the mandatory registration phase is currently in effect for non-notified Class C and D devices. The #CDSCO office has issued a circular […]
Classification and Grouping of Medical Devices & IVDs in India
Medical devices and In Vitro Diagnostic (IVD) products play a crucial role in the healthcare industry, assisting healthcare professionals in diagnosing, monitoring, and treating patients. To ensure the safety and effectiveness of these devices, governments worldwide classify and regulate them. The regulation of medical devices and IVDs in India falls under the purview of the […]
