With the rapid development of the global medical device market, the clinical requirements and regulatory policies of medical devices in the EU and China, as two major global markets, have attracted much attention. In order to help medical device companies better understand the clinical data requirements of the EU and Chinese markets, AKRA TEAM and LINKS CRO jointly held a webinar focusing on the clinical requirements of medical devices in the EU and China, bringing you the most cutting-edge industry insights and practical guidelines.
On January 17, we welcomed the annual event of Lingshi: 2025 Annual Meeting & LINKS 10th Anniversary!
On January 6, 2025, the "J-Tube™ Blood Flow Guiding Dense Mesh Stent" independently developed by Juhui Medical Technology (Shenzhen) Co., Ltd. obtained the medical device registration approval from the National Medical Products Administration! Here, we sincerely congratulate our partner Juhui Medical for taking another step forward in the field of neurointervention!
On December 16, 2024, the product "ScienCrown Transcatheter Implantable Aortic Valve System" of Lepu Xintai, a subsidiary of Lepu (Beijing) Medical Device Co., Ltd., was approved for registration by the National Medical Products Administration (NMPA)! Here, we sincerely and warmly congratulate our partner Lepu Medical for reaching new heights in the field of structural heart disease!
