Biopharma

PSUSA/00003148/202405

PSUSA/00003148/202405

AI-developed drug will be in trials by year-end, says G...

Founder of Isomorphic Labs aims to develop a drug in oncology, cardiovascular or...

China investigates generic drugs over safety concerns

Anaesthetics are not putting patients to sleep, doctors warn, in call for greate...

Drugmakers warn NHS clawback tax is putting UK at a dis...

Pharma groups say higher levy will stifle growth of life sciences

Robert Kennedy beats back anti-vax label in testy US Se...

Panel grills Donald Trump’s nominee for top health post on abortion stance and ‘...

The big haul

Putting the “loco” in relocation

AstraZeneca ditches plan to build £450mn UK vaccine plant

Decision is a blow to Starmer’s government after setting out pro-growth pitch to...

AstraZeneca rejected close to £80mn in state support fo...

UK company raised NHS rejection of its new breast cancer drug and drug pricing m...

Merck shares sink 11% after vaccine shipments to China ...

Drugmaker pauses Gardasil exports to help ‘trusted partner’ reduce excess inventory

Pfizer CEO ‘disappointed’ by Kennedy’s refusal to rebut...

Albert Bourla says Donald Trump’s nominee for health secretary still appeared to...

GSK launches £2bn buyback on strong HIV and cancer drug...

UK pharma group raises long-term annual sales forecast to more than £40bn by 2031

Rapid trials prompt deals rush for Chinese ‘super me-to...

Western drugmakers look to Chinese trials for early data on treatments’ potentia...

Meeting highlights from the Committee for Veterinary Me...

CVMP opinions on veterinary medicinal productsThe Committee adopted by consensus...

Meeting highlights from the Pharmacovigilance Risk Asse...

Medicines containing semaglutide: PRAC investigating risk of rare eye conditionP...

Human medicines in 2024

In 2024, EMA recommended 114 medicines for marketing authorisation. Of these, 46...

Revised rules on handling of competing interests published

EMA has published the revised version of its policies on the handling of competi...

New EU rules for health technology assessments become e...

EMA is ready to support the implementation of the new regulation on health techn...

Clinical Trials Regulation becomes fully applicable

From today, all clinical trials in the European Union (EU), including ongoing tr...

Meeting highlights from the Committee for Medicinal Pro...

Eight new medicines recommended for approvalEMA’s human medicines committee (CHM...

One Health: EU agencies unite to tackle azole fungicide...

For the first time, the five EU health and environment agencies – EFSA (European...

European Shortages Monitoring Platform fully operationa...

The European Shortages Monitoring Platform (ESMP) is now live with the full scop...

EMA celebrates 30 years of progress in science and medi...

EMA is celebrating 30 years of operations marking its evolving role at the centr...

Two new vaccines against bluetongue recommended for app...

EMA has recommended the approval of the vaccines Bluevac-3 and Syvazul BTV 3 to ...

FDA Approves First Acellular Tissue Engineered Vessel t...

FDA approved Symvess, the first acellular tissue engineered vessel for use in ad...

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