Advocacy Actions
Meeting with the NIFDC on the Revision of YY0341-2009
On 21st June, the delegation of the Chamber met with the National Institutes for Food and Drug Control (NIFDC) on the revision of YY0341-2009.
Read moreMeeting with the EU-China Comprehensive Agreement on Investment Negotiators on Medical Devices Sector
Representatives of the Chamber met with the EU-China Comprehensive Agreement on Investment Negotiators on Medical Devices Sector.
Read moreParticipated in the Seminar on the Administrative Measures for Mandatory National Standards (Draft for Approval)
On 13th June, the representatives of the Chamber participated in the seminar on the Administrative Measures for Mandatory National Standards (Draft for Approval).
Read moreLetter to the NMPA on the Revision of YY 0341-2009
On 4th June, the Medical Device Sector sent a lobby letter to the National Medical Products Administration, regarding the revision of YY 0341-2009, General Technical Requirements for Non-active Metallic Surgical Implants for Osteosynthesis.
Read moreComments to the IMDRF on the Proposed Update to Clinical Evaluation Documents
On 5th April 2019, the International Medical Devices Regulators Forum (IMDRF) has initiated a public consultation on the proposed update to Clinical Evaluation documents.
Read moreLetter to NIFDC on the Revision of YY 0341-2009
On 24th May, the medical device sector sent a lobby letter to the National Institutes for Food and Drug Control, regarding the revision of YY 0341-2009, General Technical Requirements for Non-active Metallic Surgical Implants for Osteosynthesis.
Read moreComments to the European Commission on the Investment Restrictions on the Medical Device Sector in China
On 21st May, the medical sector submitted comments to the European Chamber regarding the investment restrictions on the medical device sector in China.
Read moreEUCCC Innovation Centre–Dialogue on the Evaluation for Innovative Medical Devices and eRPS Kick-Off
On 17th May 2019, the European Chamber and the Centre for Medical Devices Evaluation (CMDE) of the National Medical Products Administration (NMPA), co-organized the Dialogue on the Evaluation for Innovative Medical Devices and eRPS Kick-off.
Read moreContribute to the "Green Book" of Medical Devices in China
Contribute to the "Green Book" of Medical Devices in China
Read moreMeeting on Imaging Forum and AI Medical Devices Joint Evaluation Mechanism
National Health Commission, International Cooperation Centre, (IHECC) organized a meeting with medical Imaging industry, discussing about the Medical Imaging Forum in August 2019, as well as the AI Medical Devices Joint Evaluation mechanism.
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