To unlock the new growth momentum for the IVD industry and extend its value boundaries, CACLP 2026 will, for the first time, introduce the At-Home Testing Pavilion, taking place from 21–23 March 2026 in Hall 5, Xiamen International Expo Center.

CACLP 2026 will debut the Medical Research Pavilion as a dedicated platform designed to bridge scientific research with clinical practice within the healthcare system.

On February 7, 2014, China Food and Drug Administration (CFDA) issued the Special Review and Approval Procedure for Innovative Medical Devices (interim), which will be put into force as of March 1, 2014. The Procedure is an approval channel

Company: Kyowa Medex Website: www.kyowamx.co.jp Product: Determiner L HbA1c

Company: hotgen Website: www.hotgen.com.cn Product: UPTquik® Lp-PLA2 Kit

Company: AVE Website: www.c-ave.com Product: AVE-562 Fully Automated Feces Analyzer

Company: Liming Website: www.limingbio.com Product: StrongStep® Trichomonas/ Candida Combo

Company: Liming Website: www.limingbio.com Product: StrongStep® Chlamydia trachomatis/ Neisseria gonorrhoeae Combo

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Company: Landwind Website: /uploads/allimg/180628/1ZU42P3-0.jpg Product: LW C400

The Name of Devices and Model, Name and Address of Manufacture must be unanimously the same as the contents carried in the documents approved by the government of the Country (Region) of Origin, and must be consistent with the contents concerned c

In order to implement the Medical Device Supervision and Management Ordinance (State Council Decree No. 650) and the Opinion of the State Council on the reform of drug and medical device review and approval system (Guo Fa [2015] 44), and to