In the rapidly evolving landscape of cybersecurity, particularly within the medical device and healthcare sectors, maintaining compliance with regulations and ensuring the security of products...
In the rapidly evolving world of medical devices, keeping pace with regulatory changes is essential for success. As the global regulatory landscape undergoes significant...
The NMPA issued the “Regulation on the Supervision and Administration of Medical Devices” on January 7, 2025, a revised version of the same-named regulation...
In today’s rapidly evolving regulatory landscape, medical device companies face increasingly complex challenges in managing compliance and bringing their products to market efficiently. As...
NMPA Center for Food and Drug Inspection released the “Key Points for the Inspection of Real-World Studies on Medical Devices (Draft)” for feedback on...
