NMPA: 49 Class III Devices Impacted by 2024 Guidelines Revisions Plan
Source Node: 2542994
Time Stamp: Apr 11, 2024
China Med Device
1380 Institutes Certified to Conduct Clinical Trials in China
Source Node: 2541784
Time Stamp: Apr 10, 2024
NMPA Interpretation on Device Usability Engineering Guideline
Source Node: 2538799
Time Stamp: Apr 6, 2024
NMPA Usability Engineering Guideline Issued for Medical Devices
Source Node: 2530018
Time Stamp: Mar 29, 2024
Eight Mandatory and Ninety Recommended Standards to be Revised in 2024: Revisions Plan Asks Your Feedback
Source Node: 2530020
Time Stamp: Mar 28, 2024
NMPA Review Report Released for Intuitive Surgical’s Navigational Bronchoscopy System
Source Node: 2533833
Time Stamp: Mar 28, 2024
2024 National Inspection Plan Released Today: Pay Attention to Your Device Standards
Source Node: 2521208
Time Stamp: Mar 20, 2024
Guidance Reveals How NMPA Inspects Your Clinical Trial Institution
Source Node: 2520232
Time Stamp: Mar 19, 2024
21 Class III Devices Exempted for Clinical Trial: Faster Market Access for Surgical Equipment in Cardio, Neuro, Ortho, Aesthetic and Dental Applications
Source Node: 2520236
Time Stamp: Mar 18, 2024
From April 1, RF Aesthetic Equipment Will Require Device Certificate
Source Node: 2507480
Time Stamp: Mar 7, 2024
NMPA RFA & MWA Equipment Clinical Guideline Asks Feedback
Source Node: 2499324
Time Stamp: Feb 28, 2024
Two Review Reports for Imported Devices Issued in January
Source Node: 2497343
Time Stamp: Feb 25, 2024
Medical Device Companies Annual Self-Inspection Report Due March 31
Source Node: 2494096
Time Stamp: Feb 23, 2024
NMPA Review Report Released for Israeli Osteosynthesis Plate System
Source Node: 2494100
Time Stamp: Feb 23, 2024
Clinical Trial Draft Guideline Issued for Peripheral Drug-Coated Balloon Catheter
Source Node: 2470977
Time Stamp: Feb 6, 2024
Boston Scientific, Abbott and Medtronic Have Urgent Needed Devices Designated in GBA
Source Node: 2463296
Time Stamp: Jan 31, 2024