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Decree 4 Provisions For Medical Device Registration (Expiry)

Decree 19 Good Manufacturing Practice In Class III Medical Device Manufacturers

Decree 1 Measures For The Administration Of Medical Device Adverse Event Monitoring And Re-evaluation

Decree 1 Annex 9 Guideline On Inspecting Medical Device Adverse Event Monitoring Activity (draft)

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)