Commercial Information Circulars
24-hour hotline : 23 922 922
e-mail address : enquiry@tid.gov.hk
Ref. : EIC 631/2/5
15 February 2016
Dear Sirs,
Commercial Information Circular No. 178/2016
The Mainland of China : Notice Concerning Effectively Implementing the Work on the Implementation of the "Good Manufacturing Practice for Medical Devices" by the Production Enterprises of Medical Devices (Category 3)
The China Food and Drug Administration issued on 3 February 2016 a notice concerning effectively implementing the work on the implementation of the "Good Manufacturing Practice for Medical Devices" by the production enterprises of medical devices (category 3). Please refer to the Appendix (pdf format) for the notice (available in Chinese only).
2.For details of the "Notice Concerning Issues on the Implementation of the 'Good Manufacturing Practice for Medical Devices' by the Production Enterprises of Medical Devices (Category 3)", please refer to CIC No. 177/2016 dated 15 February 2016.
ENQUIRIES
3.If you have any questions on the content of the document mentioned in this circular, please contact the issuing authority of the Mainland of China direct. For other questions on this circular, please contact Mainland Branch (I) (tel: 2398 5444) of the Department.
Yours faithfully,
(Miss Bonny CHAO)
for Director-General of Trade and Industry
Note: While every effort is made to ensure the accuracy of the above information, the Department cannot guarantee this to be so and will not be held liable for any reliance placed on the same.