The US Food and Drug Administration granted 510(k) marketing clearances for various tests to aid the diagnosis and treatment of infectious diseases, among other products.

Positive results from the DESTINY-Breast11 Phase III trial showed ENHERTU followed by paclitaxel, trastuzumab and pertuzumab, THP, in the ...

BRS working president KT Rama Rao said research must serve the common man, calling it futile otherwise. Inaugurating Huwel’s ...

Co-Diagnostics, Inc. (Nasdaq: CODX) (the "Company" or "Co-Dx"), a molecular diagnostics company with a unique, patented ...

Residual DNA Testing is vital in detecting trace DNA post-biological processes, crucial for safety across biotechnology, pharmaceuticals, and forensics. It ensures biopharmaceuticals like vaccines are ...

The Delhi Police has registered a case of gang rape following a complaint of sexual assault by an 18-year-old student of South Asian University (SAU) in Delhi. | Latest News India ...

The U.S. Food and Drug Administration has granted an emergency use authorization for a COVID-19 test from Alphabet Inc unit Verily Life Sciences.

Seven months after Brazil declared a state of emergency because of the new coronavirus pandemic, the country's Health Ministry has distributed less than a third of the 22.9 million available RT-PCR ...

A research team in Japan has developed an innovative system that can accurately detect genetic mutations in brain tumors ...

Overview of the process of obtaining genomic diversity of influenza virus in a population replicated from a single particle. (a) MDCK cells were infected with influenza vi ...