License For Conducting Clinical Investigation in India: A Guide
Medical device manufacturers/importers who wish to conduct a clinical investigation in India need to obtain permission from the CLA. The CLA is the Central Licensing Authority (CLA) and functions under the CDSCO. The CDSCO is the Central Drugs Standard Control...
Notified and Non-Notified Medical Devices: Key Differences
In this blog, we have focused on the differences between notified and non-notified medical devices in India. Additionally, we have provided an overview of the different regulatory processes for different categories of medical devices. Furthermore, we have touched upon...
National Single Window System (NSWS) Portal: An Overview
With the consistent rise in demand for medical devices and pharmaceuticals, a streamlined regulatory approval system was very necessary. Moreover, India is aiming to become the global hub for medical devices and pharmaceuticals. Thus, a platform for seamless and...