
Moderna has announced that its coronavirus vaccine candidate has shown promise in generating an immune response in elderly patients in …

The FDA has given emergency clearance for Abbott’s portable COVID-19 test that it will sell for just $5. The company’s …

Canada is set to roll out automated drug dispensers that can provide clean, doctor-prescribed medicine to opioid addicts by scanning …

Thousands of coronavirus cases are thought to have been transmitted within UK hospitals, according to a new study. Researchers at …

The US Department of Justice (DOJ) has charged Teva Pharmaceuticals with conspiracy to fix the price of its generic drugs. …

A 75-year-old woman from Nottinghamshire is thought to be the first British case and victim of COVID-19. She tested positive …

The Africa Regional Certification Commission has declared Africa to be free from wild polio. Nigeria, Pakistan and Afghanistan were the …

“Every company is different, so you have to be open-minded and receptive to the culture when joining.” Can you briefly …

In COVID-19 news this week, China is set to move ahead with human testing of a potential coronavirus vaccine that …

The World Health Organization has warned that the use of blood plasma from coronavirus patients to treat COVID-19 is still …

Novavax has started to enroll volunteers into the second phase of testing its COVID-19 vaccine candidate. The Phase 2 trials …

A man in Hong Kong has been reinfected with the coronavirus, stoking fears that immunity to the virus may be …

The FDA has granted Lupin Ltd approval for their generic version of ProAir, which is used to prevent asthma symptoms …

AstraZeneca has started a clinical trial of its antibody treatment designed to prevent and also treat symptoms of coronavirus. The …

AstraZeneca and RenalytixAI have agreed a deal to develop joint precision medicine strategies for cardiovascular, renal and metabolic diseases. The …

China is set to move ahead with human testing of a potential coronavirus vaccine that has been created using insect …

The FDA could expand its Emergency Use Authorization (EUA) for Gilead’s remdesivir for treating coronavirus patients, according to Gilead.

The FDA has approved a request from American Gene Technologies to begin a clinical study into its HIV gene therapy. …

The FDA has issued an Emergency Use Authorization (EUA) for convalescent plasma to treat patients with COVID-19. The regulatory body …

The FDA has approved Genmab and Janssen’s Darzalex (daratumumab) as a treatment for relapsed and refractory multiple myeloma, when combined …