
More than two thirds of black, Asian and minority ethnic pharmacists have not had any workplace risk assessments for COVID-19, …

In a crucial step amidst the ongoing pandemic, the European Medicines Agency’s Committee for Medicinal Products for Human Use (CHMP) …

The news this week centres on the pandemic in Europe, with the Independent SAGE group are warning that it is …

AstraZeneca has continued to build its manufacturing capacity to deliver its COVID-19 vaccine candidate, developed in partnership with the University …

Novartis’ Mayzent (siponimod) has been unsuccessful in securing a recommendation from NICE for use on the NHS for the treatment …

A new study has highlighted how human biases affect the regulatory approval process of the FDA.

Coronavirus antibody tests that are beginning to be used by NHS and care staff have been distributed without adequate assessment, …

The National Institutes of Health had its funding cut from a research project into bat coronavirus, according its Director Dr …

Gilead has announced its intention to acquire 49.9% of shares in cancer immunotherapy specialist Pionyr Therapeutics with a payment of …

British Prime Minister Boris Johnson announced an extensive rollback of existing lockdown measures to restrict the spread of COVID-19 in …

Coronavirus news this week sees treatments for existing diseases being tested in COVID-19 patients, with Roche’s rheumatoid arthritis drug Actemra …

Johnson & Johnson have had a bid to overturn a verdict that blamed the company’s baby powder for giving women …

The Home Office has announced that the drug Epidyolex (cannabidiol) has been reclassified as a Schedule 5 drug, a move …

Boehringer has revealed that it intends to withdraw its investment from Hikma Pharmaceuticals, with the company poised to sell 28 …

The UK’s Medicines and Healthcare products Regulatory Agency (MHRA) has extended Santhera’s Duchenne muscular dystrophy (DMD) drug Puldysa (idebone) for …

Sanofi has said it expects to have its coronavirus vaccine approved by the start of next year which is faster …

Gilead is intent on pushing the applications of its antiviral drug remdesivir after it has shown efficacy in the treatment …

Senior officials from the US Food and Drug Administration and the European Medicines Agency have pledged to continue working closely …

The COVID-19 pandemic has altered the life of just about everyone, especially patients in receiving continued treatment and care. But …

China’s National Medical Products Administration (NMPA) has moved to approve a 300mg pre-filled pen formulation of Sanofi and Regeneron’s Dupixent …