MED-(Chinese version) Announcement on Issues Related to Administrative Acceptance of Medical Devices During the Transitional Period of Regulations

MED-(Chinese Version) Provisions for MD AE monitoring and Re-evaluation (for Trial Implementation)

MED-(Chinese version) Announcement on Matters Related to the Seal of In Vitro Diagnostic Reagents Clinical Trial Institutions

MED-(Chinese version) Announcement on the Use of Acceptance and Certification, Technical Review and Administrative Examination and Approval Subsystems of Medical Device Registration Management Information System