NMPA Registration

NMPA Registration

According to Measures for Supervision and Administration of Medical Device Manufacturing

 issued by NMPA, firms who manufacture Class II and/or Class III medical devices in China

 shall obtain Medical Device Production License.

According to Measures for the Administration of Medical Device Registration issued by NMPA,

 firms who are intended to commercial distribute medical devices (domestic or import devices) in China shall obtain the Medical Device Registration License. Imported medical devices shall be

granted with registration license by NMPA.

Services 

 Application strategy consulting and establish application protocol.

 Prepare product technical requirements

 Complete the registration dossier

 Communication with corresponding administration

 Assist you in obtaining Medical Device Distributing License

 Assist you in obtaining Medical Device Production License (domestic firms)

 Act as your Legal Agent (overseas firms)

Registration Procedure