Advocacy Actions
Submitted comments to NIFDC on two draft guidelines for Full Safety Assessment
Submitted comments to NIFDC on two draft guidelines for Full Safety Assessment
Read moreSubmitted comments to NIFDC on two draft guidelines for Full Safety Assessment
Submitted comments to NIFDC on two draft guidelines for Full Safety Assessment
Read moreEuropean Chamber Roundtable with Lingang Data Division
On 7th April, the European Chamber and the Data Division of the Lingang Management Committee held a roundtable in Lingang to discuss the Lingang’s pilot measures for the cross-border data transfer (CBDT).
Read moreEuropean Chamber Secretary General Meets Assistant Minister of IDCPC
On 27th March, Secretary General Adam Dunnett attended a closed-door roundtable hosted by Assistant Minister Zhao Shitong of the International Department of the Communist Party of China (IDCPC), to provide feedback on China’s business environment.
Read moreParticipated a meeting on optimization measures discussion for full safety assessment implementation led NMPA
Participated a meeting on optimization measures discussion for full safety assessment implementation led NMPA
Read moreEuropean Chamber meets the Department of Commerce of Guangdong Province
On 26th March 2024, the European Union Chamber of Commerce in China participated a roundtable discussion hosted by Director General Zhang Jinsong of the Department of Commerce of Guangdong Province in Beijing.
Read moreThe Consumable and Disposable Medical Device Advisory Committee and the COCIR Registration Affairs Taskforce Submitted a Letter to the National Medical Products Administration on the Issues of Product Service Life and Dynamic Management
The Consumable and Disposable Medical Device Advisory Committee and the COCIR Registration Affairs Taskforce have written to the National Medical Products Administration. They expressed concern about equating a product's service life with product failure, clarifying that the term "service life" should be interpreted as "expected service life". They also proposed that medical device end users should be allowed to manage the "expected service life" of their devices dynamically, potentially extending the use of products beyond their "expected service life" based on regular evaluations and maintenance records.
Read moreWG Chair participated the Full safety assessment meeting with NMPA & NIFDC
Full safety assessment meeting with NMPA & NIFDC
Read moreFeedback Submitted to Chongqing Municipal Healthcare Security Administration on Chongqing Basic Medical Insurance Payment Methods by Disease Related Group (DRG) (Draft for Comments)
The Healthcare Equipment Working Group provided feedback to the Chongqing Municipal Healthcare Security Administration on Chongqing Basic Medical Insurance Payment Methods by Disease Related Group (DRG) (Draft for Comments).
Read moreSeminar with China Academy of Information and Communications Technology (CAICT)
The COCIR Desk had a meeting with the China Academy of Information and Communications Technology (CAICT) on the 21st of March.
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