From 16 to 18 March 2024, the bustling halls of Chongqing International Expo Center witnessed a remarkable convergence of innovations and advancements, as the 21st China Association of Clinical Laboratory Practice Expo (CACLP) and the 4th edition of China IVD Supply Chain Expo (CISCE) concluded with resounding success.
With the rapid development of technology, in vitro diagnostics (IVD) is playing an increasingly important role in the field of medicine. The application of next-generation technologies such as molecular biology, genomics, immunology, and others has not only increased the sensitivity and specificity of diagnostics but has also made the detection, diagnosis, and monitoring of diseases more accurate, rapid, and personalized. *Simultaneous interpretation (CNH/EN) is provided onsite.
Company: Liming Website: www.limingbio.com Product: StrongStep® Chlamydia trachomatis/ Neisseria gonorrhoeae Combo
Company: Landwind Website: www.landwind.com.cn Product: LW D6580
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
In order to implement the Opinions of the State Council on the Reform of Examination and Approval System for Medicine and Medical Devices (Guo Fa [2015] No. 44) and the reform spirit of relevant administrative examination and approval syste
A.TheDirectionfortheApplicationFormofRegistration 1.AllthecontentsfilledinshallbeinbothChineseandEnglish; 2.Upontheapplication,theformshallbeprinted; 3.Alltheitemsmustbecompletelyfilledin,andasforthevacantitems,ldquo;/rdquo;shallbeusedt
China Food and Drug Administration (CFDA) recently released the 2014 Drug Review Annual Report. The Annual Report describes the general situation of drug registration acceptance, review and approval in 2014, and analyzes the data of accepta
A. The Direction for the Application Form of Registration 1.All the contents filled in shall be in both Chinese and English; 2.Upon the application, the form shall be printed ;
Article 1 These Regulations are hereby formulated with a view to strengthening the supervision and administration of medical devices, ensuring their safety and effectiveness and protecting human health and life safety.
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