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Decree 1 Annex 7 Guideline On Focus Points When Monitoring Medical Device Adverse Events (draft)

Decree 1 Annex 5 Collection And Reporting Of Medical Device Adverse Events For Marketing Authorization Holder Guiding Principles (draft)

Decree 1 Annex 3 Guideline On Medical Device Adverse Event Monitoring Scope (draft)

Decree 1 Annex 1 Guideline On Medical Device Adverse Event Monitoring (draft)

Customized Additive Manufactured Medical Device Submission Technical Review Guidance (Draft)

Clinical Trials Guidelines For Companion Diagnostic Reagents For Approved Anti-tumor Drugs (draft)

Clinical Exemptions Cancer Biomarkers

Chinese Pharmacopoeia- 1110 Biological Tests- 1101 Sterility Test(1)

CRP Assay Kit Registration Technical Review Guideline

Announcement On Record Filling Of Medical Device Master Files

Amendment To Decree 680 Regulations On Supervision And Management Of Medical Devices (Expiry)

Adverse Event Monitoring Guideline For Medical Device Registrant