CMDE is soliciting participation in the revision and preparation of the “Guidance for Registration Review of Platelet-rich Plasma Preparation Device” and the “Guidance on Conditional Approval of Medical Devices (2024 Revised Edition)”. It invites domestic and foreign manufacturers, research institutions, and clinical institutions with relevant experience to actively participate.
Interested parties are invited to fill out the Participation Information Collection Form for the revision and preparation work and submit the completed form electronically to the CMDE by July 26, 2024.