Through harnessing innovations in its regulatory processes, including digital transformation in health care, BPOM is ...

Received 3 Rare Pediatric Disease Designations (RPDD) from FDA for each of 3 potential therapies for 3 different rare inherited retinopathies including AAV-AIPL1 Agreed on pathway with MHRA for ...

More collaborative initiatives are taking place among regulatory agencies, health technology assessment (HTA) bodies and ...

Last week, the US Food and Drug Administration (FDA) claimed that a core component in many popular nasal decongestants is ...

A daily pill designed to help people give up smoking will soon be rolled out on the NHS as experts hope it could prevent ...

Pinnacle’s General Oral Solids facility in Baddi is a world-class manufacturing hub designed to meet and exceed global ...

Dr Oscar Duke has spoken on BBC Morning Live about the recent concerns surrounding a popular cold and flu component, as the ...

Johnson & Johnson has announced that the Medicines and Healthcare products Regulatory Agency (MHRA) has granted marketing authorization for BALVERSA®▼ (erdafitinib) as a monotherapy for the treatment ...

"Generic drugs are used around the world. There are no doubts about their safety and efficacy as they have undergone ...

WARRINGTON and Halton Hospital are looking for over 60s to take part in a norovirus vaccine trial. Norovirus is one of the most common causes of stomach bugs in the UK and there is currently no ...

The National Institute for Health and Care Excellence (NICE) has recommended Blueprint Medicines’ Ayvakyt (avapritinib) to ...

should be registered with the MHRA (Medicines and Health care products Regulatory Agency) prior to being released onto the ...