Advocacy Actions
Meeting with the Shanghai Customs on Medical Device Customs Clearance Inspections Issues
On 17th July, the medical device sector visited the Shanghai Customs for medical device customs clearance inspections issues.
Read moreInternational Medical Device Regulator Forum (IMDRF) Working Group Meeting on Documents for Clinical Evaluation and Investigation
On 9th July, International Medical Device Regulator Forum held a working group meeting on clinical evaluation.
Read moreSupport Letter for the Applications for Punitive Tariff Exclusions to the Ministry of Finance
The Tariff Commission of the State Council, which responsibilities are served by the Ministry of Finance, started the tariff exclusions on 13th May.
Read moreSent the Industrial Analysis on the Main Tasks of 2019 on Deepening Reform of the Medical and Healthcare System to the Delegation of the European Union to China
On 26th June, the medical devices sector sent the industrial analysis on the Main Tasks of 2019 on Deepening Reform of the Medical and Healthcare System to the Delegation of the European Union to China.
Read moreMeeting 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 more