Germany's authority, the Federal Institute for Drugs and Medical Devices, oversees the registration process for medical devices. Importers of such items must adhere to detailed guidelines to ensure the quality and performance of their offerings. Key requirements include {pre-market notification, a comprehensive product file, and post-market surve… Read More

Medical device import registration in India can be a complex process. Companies seeking to supply their products into the country must comply with stringent regulations. A successful import journey often requires careful planning and engagement with relevant authorities. Key steps include performing a thorough analysis to identify market opportuni… Read More

Securing authorization for medical devices in India involves a structured procedure. Regulatory bodies, like the Central Drugs Standard Control Organization (CDSCO), oversee this terrain. Potential manufacturers must meet stringent standards that ensure the safety and integrity of their products. The approval process often involves a series of sta… Read More