Quidel (Nasdaq:QDEL) announced today that it completed its $6 billion acquisition of Ortho Clinical Diagnostics (Nasdaq:OCDX).

Monkeypox is a zoonotic disease that was first identified in monkeys in 1958. Although it is named monkeypox virus, its primary host is rodents such as mice and squirrels, and its opportunistic host is primates, humans.

DoMore Diagnostics has obtained the CE mark for its Histotype Px Colorectal deep-learning algorithm to predict colorectal cancer patient outcomes based on the analysis of digital histology images, enabling its clinical use in the European Union and other geographies that accept the designation.

The World Health Organization has received reports of 257 confirmed monkeypox cases and about 120 suspected cases in 23 nations where the virus is not endemic as of Thursday, it said in a Sunday update.

In the face of the sudden monkeypox virus epidemic, many Chinese in vitro diagnostic enterprises responded quickly, completed the R & D and launched the monkeypox virus nucleic acid detection kit at the first time, effectively helping overseas to carry out the monkeypox virus prevention.

Biotech firms experienced a banner year in 2020.The COVID-19 pandemic highlighted the value of innovative medical solutions, leading to new opportunities for researchproduct approvaland funding

Becton Dickinson announced on Thursday that it has obtained the CE-IVD mark for a combined influenza, SARS-CoV-2 assay. The multiplexed RT-PCR test runs on the firm's high-throughput BD Cor system.

Roche on Wednesday said the company and its unit have developed three test kits to detect the monkeypox virus, as the disease spreads in regions outside Africa.

On May 23, 2022, Autobio Diagnostics Co., Ltd. announces CE mark for AutoMeloc Monkeypox nucleic acid detection kit (PCR-fluorescent probe method).

Global life sciences leader Cytiva is opening a new 7 400m2 manufacturing facility in Grens, Switzerland on May 31, 2022. The site will manufacture single use kits for the Sepax and Sefia cell processing systems, as well as consumables for Xuri cell expansion systems.

Aiforia Technologies said Wednesday that it has received CE-IVD marking for an artificial intelligence model that helps detect progesterone-positive tumor cells.

Hologic announced Wednesday it has obtained CE marking for its Panther Fusion EBV Quant Assay and Panther Fusion BKV Quant Assay, expanding its transplant pathogen monitoring menu on the automated, real-time PCR Panther Fusion system.

On May 19, the COVID-19 Antigen Rapid Test (colloidal gold method) independently developed by Guangzhou Weimi Bio-Tech Co., Ltd (“Weimi Bio-Tech”) successfully obtained the EU CE certificate.

Illumina said on Tuesday that it has added a companion diagnostic indication to its in vitro diagnostic TruSight Oncology (TSO) Comprehensive (EU) test.

Agilent Technologies reported after the close of the market on Tuesday that its fiscal second quarter revenues rose 5 percent year over year.