Draft of New Extracellular Vesicle Regulations Released

In line with regulatory trends, our association has worked with the competent authority to propose a draft set of regulations for extracellular‑vesicle medicine, covering manufacturing standards, clinical‑safety monitoring, and ethical guidelines.

Key points of the draft:
• Certification of clinical‑grade EV manufacturing processes
• Principles of informed consent
• Data‑privacy protection

The draft is open for public comment—everyone is welcome to join the discussion.