China has been engaged in the R&D and manufacturing of semi-automatic coagulation analyzers for over a decade, and based on the data from the website of the NMPA, in 2024 and 2025 (as od 15 August), a total of 2 instruments from 2 manufacturers have obtained registration certificates...
Stay up-to-date with the latest happenings in the rapidly evolving field of In Vitro Diagnostics (IVD) in China. Latest news
British life science reagents and tools company Abcam said recently that it has signed an agreement to use BrickBio's proprietary bioconjugation platform to develop research and diagnostic products.
Invitae said recently that it will acquire Clear Genetics, a developer of software that supports the delivery of genetics services at scale, for approximately $50 million.
Expedeon announced recently that it has agreed to sell its immunology and proteomics businesses to UK-based life science reagents and tools company Abcam for €120 million ($130.0 million) in cash.
Castle Biosciences reported after the close of the market recently that its third quarter revenues skyrocketed 300 percent year over year due to growth in the firm's DecisionDx- Melanoma test report volume.
Liquid biopsy firm Lexent Bio recently announced a non-exclusive partnership with Illumina to develop an in vitro diagnostic kit for cancer.
Duke University Researchers have developed a new detection tool that uses tiny circuits made of DNA to identify cancer cells. The researchers fashioned the simple circuits from interacting strands of synthetic DNA that are tens of thousands
Renovia has received a nod from FDA for a next-generation pelvic digital therapeutic. The Boston-based company said the Ieva device is cleared for the strengthening of pelvic floor muscles and the treatment of stress, mixed, and mild to mode
Patients interested in testing themselves at home for sleep apnea now have a few more options.
Medtronic filed an amendment Tuesday to its lawsuit against Axonics Modulation Technologies, adding three more patent infringement claims to the suit. The original lawsuit, filed earlier this month, alleged infringement of four patents relat
FDA is encouraging manufacturers to reduce the amount of paper included in sterile device packaging in order to reduce the amount of ethylene oxide (EtO) required for effective sterilization. A new voluntary master file program also aims to
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