Different medical institutions have selected different imported and domestic brand instruments: 38 domestic and 58 imported.

Stay up-to-date with the latest happenings in the rapidly evolving field of In Vitro Diagnostics (IVD) in China.

Recently, Gofar issued a report (draft) on the acquisition of KOALSON, proposing to purchase the 99.9779% of KOALSON's shares held by eight people with the transaction price of about 356 million yuan by issuing shares and paying cash.

In Sep. 16th, Zhejiang Gongdong Medical Technology Co., Ltd. successfully listed on SSE (Shanghai Stock Exchange).

Recently, Gilead Sciences announced that it has reached a definitive agreement with the American biotechnology company Immunomedics (Nasdaq: IMMU).

Beijing Bohui Innovation Biotechnology acquires a total of 50% of ABIOQUANT BIO-MEDCAL TECHNOLOGY with RMB 24 million in cash.

A-share spin-off listing set off a crazy trend recently. According to Securities Daily, till Aug. 13, exceeding 40 listed companies planned to spin-off listing.

According to 2019 China In Vitro Diagnosis Industry Report, the size of Chinese IVD market in 2019 exceeded RMB 90 billion (over US$ 12.8 billion), with a growth of about 15%. Among them, imported products account for about 55% in the overal

In Biomicrofluidics, by AIP Publishing, scientists report a membrane-based invention that can concentrate the virus content of a sample of urine or saliva, allowing it to be detected.

Researchers have demonstrated a prototype of a rapid COVID-19 molecular test and a simple-to-use, portable instrument for reading the results with a smartphone in 30 minutes, which could enable point-of-care diagnosis without needing to send

FDA will not require developers to submit a premarket approval application, premarket notification or emergency use authorization for laboratory developed tests, the Department of Health and Human Services announced on August 19th.

The U.S. Food and Drug Administration issued an emergency use authorization (EUA) for investigational convalescent plasma for the treatment of COVID-19 in hospitalized patients as part of the agency’s ongoing efforts to fight COVID-19.