China National Medical Product Administration (NMPA)  has recently published a notice for “The guidelines of registration technical review on the shelf life of active medical device” with the objectives to strengthen the medical device registration workflow of inspection and principle and to improve the review quality of the registration.

For the regulatory and clinical support in regard of individual guideline, as well as translated English version of the guideline, kindly reach out to global@osmundacn.com.

Original article: https://www.cmde.org.cn/CL0056/19155.html