Germany's regulatory body, the Federal Institute for Drugs and Medical Devices, oversees the approval process for medical devices. Manufacturers of such items must comply with strict rules to ensure the efficacy and performance of what they sell. Essential aspects of the process involve {pre-marketauthorization, a comprehensive technical document… Read More

The South Asian medical device industry is experiencing substantial development. This phenomenon presents both possibilities and obstacles for entities seeking to penetrate the market. A key prerequisite for access is navigating the demanding process of medical device registration. Achieving authorization from the relevant agencies is mandatory fo… Read More