It was licensed under restricted use in clinical trial mode, where detailed safety reporting was carried out for several hundred thousand subjects. The safety of Covaxin was also evaluated by the ...

London: Amgen on Thursday said it was very encouraged after completing an interim analysis of its mid-stage study of experimental weight-loss drug MariTide and will no longer develop its oral obesity ...

Dr Reddy's Laboratories on Friday said it has launched a generic medication, used to treat a wide variety of bacterial infections, in the US market. The company has launched Doxycycline Capsules (40 ...

Aurobindo Pharma Ltd on Friday said it has received tax demand of over Rs 13 crore, including interest and penalty, from the GST authority over ineligible input tax credit claim. The Deputy ...

Washington: The lungs' blood arteries differ from those of the rest of the body. This distinction is obvious in pulmonary hypertension, in which only the lungs' blood arteries harden gradually, ...

With the move, an estimated 100,000 previously uninsured participants in the Deferred Action for Childhood Arrivals program, ...

Transcarent, which was founded in 2020, helps companies to cut costs and effectively manage health care benefits for their employees by reducing complexity. More than 4.3 million people have access to ...

France inscribed the guaranteed right to abortion in its constitution in a world first this year, sending a powerful message of support to women around the globe. Meanwhile, Poland's parliament held a ...

This is Maiva's first private equity fundraise and the proceeds will be used to set up a new manufacturing facility near ...

Valadez's case is one of tens of thousands against GSK, Boehringer Ingelheim and other pharmaceutical companies, which have worried investors in recent years. It will offer the first test of whether ...

The establishment of both the kidney transplant facilities and the iron removal plant is part of the government's broader strategy to improve healthcare services across the state, with ongoing ...

The U.S. Food and Drug Administration will decide whether to approve Moderna's RSV vaccine, currently dubbed MRNA-1345, by the end of next week. The CDC's panel of external advisers will then vote in ...