Merck on Friday said the recommendation from the European Medicines Agency's Committee for Medicinal Products for Human Use covers the 21-valent conjugate vaccine for immunization for the prevention ...

Merck & Co. said a key European regulatory committee has ... Merck on Friday said the recommendation from the European Medicines Agency's Committee for Medicinal Products for Human Use covers ...

Scholar Rock submitted its BLA of apitegromab for the treatment of patients with Spinal Muscular Atrophy with a request for ...

A group of Estonian psychiatrists and civic activists believe that allowing the therapeutic use of currently prohibited ...

SAN DIEGO--(BUSINESS WIRE)--Acadia Pharmaceuticals Inc. (Nasdaq: ACAD) today announced that the company has submitted a Marketing Authorization Application (MAA) to the European Medicines Agency ...

The continued shift towards telemedicine and remote hyper-personalized care elevates the role of digital and communications technologies as key components ... EU’s European Medicines Agency ...

Pharma: Launch of Shortages Monitoring Platform, several Changes re Clinical Trial Management in EU Countries; Devices: Resolution on the need ...

Q4 2024 Earnings Call Transcript February 4, 2025 Merck & Co., Inc. misses on earnings expectations. Reported EPS is $1.72 ...

While the person is given malaria treatments ... of the disease received a ‘positive opinion’ from the European Medicines Agency — a form of approval for drugs that will be used outside ...

was approved by the Medicines and Healthcare products Regulatory Agency (MHRA) as a treatment for moderately to severely active UC, a few weeks after it was cleared by the European Commission.

Improved analytical techniques mean tiny amounts of endocrine disrupting compounds or PFAS can be found in many places. But ...