國家藥品監督管理局醫療器械法規流程需知

日期及時間

日期: 2020-08-07
時間: 10:00am – 12:45pm

摘要

Planning to sell your medical device (including in vitro diagnostic (IVD) device) in Mainland China? 
If so, you will need to register and file them with the relevant regulatory authority, the National Medical Products Administration (NMPA) (formerly the China Food and Drug Administration (CFDA)).
What should R&D companies in Hong Kong do before beginning the registration process?

The HKSTP BioMedical Technology (BMT) Cluster and TecONE will organize a webinar on the
latest updates on essential topics related to the NMPA registration process, followed by one-on-one consultation sessions with experts. 

語言

Mainly in English (Mandarin by some speakers)


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