
NMPA Guidance on Medical Device Registration
The new article provides an overview of the revised guidance dedicated to registration of medical devices intended to be marketed and used in China.
The new article provides an overview of the revised guidance dedicated to registration of medical devices intended to be marketed and used in China.
The article describes in detail the approach to be followed by the parties involved in operations with digital medical devices in order to ensure the safety and proper performance of their products
This article was updated June 2, 2025. In this article, we will provide a comprehensive introduction to Class III medical devices, including what they are, how they are regulated, and what makes them different from other classifications. Whether you are a healthcare...
The new article describes in detail the approach to be applied with respect to documentation related to informed consent. Table of Contents Class II medical devices are an important segment of the medical device industry.These moderate-risk devices include many...