MEDICAL DEVICE

Customs Simplifies Exit Paperwork for Medical Devices

23 July 2021

The General Administration of Customs announced on 8 July that the record-filing form and the free sale certificate issued by drug supervision and administration department for the export of medical devices and medical device products may now be used to apply for sanitation and quarantine certification for the exit of special articles. More

hktdc research

Revised Regulations on Medical Devices To Take Effect in June

08 April 2021

New Regulations on the Supervision and Administration of Medical Devices, recently revised and promulgated by the State Council (State Council Decree No. 739 [2021]), will take effect on 1 June 2021. More

hktdc research

Start-Up Hong Kong: “Made in Hong Kong” Helps Instill Consumer Trust

28 October 2020

Beluntech focuses on developing medical devices and AI systems for monitoring various chronic diseases. Its CEO Lydia Leung talked about why the company insisted on establishing its production line in Hong Kong, and the new opportunities brought about by Covid-19. She also discussed the Greater Bay Area, which she hopes will lead to increasing alignment in medical device regulations between the mainland and Hong Kong. More

hktdc research

CFDA Adjusts Administrative Approval Procedures for Medical Devices

18 April 2017

In a bid to optimise the workflow and efficiency of the evaluation and approval of medical devices, the Decision of the China Food and Administration (CFDA) on Adjusting Some Administrative Approval Procedures for Medical Devices (CFDA Order No.32) will take effect on 1 July 2017. More

hktdc research

CFDA Adjusts Administrative Approval Procedures for Medical Devices

18 April 2017

hktdc research

China Adds 151 Items to Cross-Border E-Commerce Retail Imports List

21 April 2016

Chinese state authorities including the Ministry of Finance and the National Development and Reform Commission jointly released the List of Cross-Border E-Commerce Retail Imports (Second Batch), effective 16 April. More

hktdc research

China Issues Amended Good Manufacturing Practice for Medical Devices

28 January 2015

The China Food and Drug Administration (CFDA) recently amended the Guidelines of Good Manufacturing Practice for Medical Devices to strengthen supervision over the production of medical devices. More

Page of 2