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...
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...
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...
Setting up a pharmaceutical manufacturing company is a daunting task. To establish a pharma company, you need to set up a manufacturing facility equipped with various machineries and equipment. It is important to choose the appropriate pharmaceutical manufacturing...
Medical device grouping has been introduced to enhance the license application process in India. Grouping of medical devices expedites and simplifies the CDSCO registration and license application process. In this blog, we will delve into the grouping of medical...