Surgical patients may still have leftovers in their system even after a standard fast, potentially increasing the chance of a serious complication.

Zevra to receive a 2025 New Treatment Award for MIPLYFFA™ at the 21st Annual WORLDSymposiumEight abstracts discussing data and clinical ...

The regulatory frameworks in the life sciences and healthcare sector keep evolving rapidly and dynamically. Several important legislative reforms ...

GSK (NYSE:GSK) announced Tuesday that the EU drug regulator has agreed to review depemokimab, an experimental monoclonal antibody targeting a class of cell signaling molecules called interleukin-5, ...

ImmunityBio (IBRX) announced the European Medicines Agency has accepted for review and begun assessing the marketing authorization application ...

Acadia Pharmaceuticals ACAD announced that it has submitted a marketing authorization application (MAA) to the European Medicines Agency (EMA) seeking approval for trofinetide to treat Rett syndrome ...

"We're looking for our EDGE firm to be out there recruiting, bringing new business to Oklahoma, helping them find incentives that work well at the state level, and again, partner with our CORE ...

Some medicines need to be given at a certain time to make sure ... like syndrome - a rare but serious condition with symptoms of fever, altered mental state, muscle rigidity, increased heart rate and ...

The EES scheme is different to the European Travel Information and Authorisation Scheme (ETIAS), which will run alongside the former and require British travellers to apply for a visa waiver to ...

President-elect on Friday Donald Trump named Tammy Bruce, a Fox News contributor and host, as the next spokesperson for the State Department. "It is my great honor to announce that Tammy Bruce ...

The European Medicines Agency (EMA) announced that it will review 2 Danish studies which indicate there may be a link between semaglutide injection drug Ozempic (Novo Nordisk) and non-arteritic ...