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Management Provision On The Self-Testing For Medical Device Registration (Final)

Writing Specification For Periodic Risk Evaluation Report Of Medical Devices (NMPA No.46 2020)(Final)

NMPA Notice On Expansion Of The Pilot Medical Device MAH

Regulation On The Supervision And Administration Of Medical Devices 2021 (Final)

Technical Guideline Of Clinical Evaluation Report For Medical Device Registration (Final)

Rules For Unique Device Identification

Record Filing Requirement Of Medical Device Master Files

Operation Specification For Record Filing Of Medical Device Master Files

Interim Measures For The Administration Of Human Genetic Resources

Guideline For Record Filing Of Medical Device Master Files

Decree 83 Innovation Approval Procedure

Decree 131 Announcement On Using Chinese Name For Registrant Or File Submitter Of Imported Medical Devices