Technology Transfer in Medical Devices: The What and Why
The Indian medical devices industry is dynamic and evolving. India is witnessing an increasing demand for technologically advanced novel medical devices. Technology transfer increases local production, thereby increasing access to advanced medical devices. Medical...
SaMD and SiMD: The Differences and Applicable Regulations
New-age technology and software are revolutionizing healthcare. Currently, software is being used to monitor, diagnose, prevent, manage, and even treat diseases. Software used in healthcare industry are available in different types and forms. The two main categories...
CDSCO License Retention Fee: Mandatory for License Validity
In a recent circular, dated 15.5.24, CDSCO has issued a reminder for license or registration retention under MDR, 2017. This reminder for license and registration certificate renewal requirements is intended for medical device manufacturers, importers, and testing...
Medical Device Process Validation Assures the Device Quality
Regulatory bodies require medical device manufacturers to confirm whether the finished product meets the set regulatory benchmark. Manufacturers need to have strict quality control systems to ensure the devices being manufactured comply with safety and quality...