Biopharma

Human medicines European public assessment report (EPAR...

Human medicines European public assessment report (EPAR): Onureg, azacitidine, D...

Basilea opts not to take MRSA antibiotic into clinic du...

Basilea Pharmaceutica has cited its “stringent risk-return criteria” as a reason...

Opinion: What my sister’s life and death taught me abou...

“A decade ago this past June, my sister died at the National Institutes of Healt...

The lasting human impact of Trump funding freeze: An 86...

The uncertainty around the spending freeze was an epiphany for some, a realizati...

STAT+: XRHealth makes another acquisition, aiming to b...

XRHealth is acquiring RealizedCare, a company that couples immersive experiences...

Onureg : EPAR - Procedural steps taken and scientific i...

Onureg : EPAR - Procedural steps taken and scientific information after the auth...

European Medicines Agency’s data protection notice rega...

European Medicines Agency’s data protection notice regarding personal data proce...

Maximum residue limits (MRL)

Maximum residue limits (MRL)

EMEA-003155-PIP01-21-M01

EMEA-003155-PIP01-21-M01

EMA Open Door Day, European Medicines Agency, Amsterdam...

EMA Open Door Day, European Medicines Agency, Amsterdam, the Netherlands, from 9...

Human medicines European public assessment report (EPAR...

Human medicines European public assessment report (EPAR): Azacitidine Accord, az...

ACT EU workshop on ICH E6 R3 (principles and Annex 1) ,...

ACT EU workshop on ICH E6 R3 (principles and Annex 1) , Online, European Medicin...

Programme - EMA's Open Door Day

Programme - EMA's Open Door Day

Agenda - ACT EU workshop on ICH E6 (R3)

Agenda - ACT EU workshop on ICH E6 (R3)

FDA Approves Merilog (insulin-aspart-szjj), a Biosimila...

February 14, 2025 -- Today, the U.S. Food and Drug Administration approved Meril...

STAT+: STAT is backing up and monitoring CDC data in re...

STAT is backing up and monitoring CDC data in real time: See what's changing.

FDA Approves Xbryk (denosumab-dssb), a Biosimilar to Xgeva

INCHEON, Korea – Feb 16, 2025 – Samsung Bioepis Co., Ltd. today announced that t...

STAT+: Drug inspectors, AI experts, maternal health wor...

"Read this email immediately” That was the subject line of emails that landed in...

Lundbeck’s Potential Treatment Amlenetug for Multiple S...

Wed, Feb 12, 2025 -- The FDA has granted Fast Track Designation to Lundbeck’s in...

At premier science gathering, ‘anger, uncertainty, and ...

At the AAAS annual meeting, "anger, uncertainty, and anxiety" about the future o...

STAT+: CDC cuts expected to devastate Epidemic Intellig...

Members of the CDC's Epidemic Intelligence Service were warned Friday that many ...

FDA Grants Fast Track Designation to PleoPharma, Inc's ...

PHOENIXVILLE, Pa., Feb. 13, 2025 /PRNewswire/ -- PleoPharma, Inc., a privately h...

Innate Pharma Announces U.S. FDA Granted Breakthrough T...

February 17, 2025 -- Innate Pharma SA (Euronext Paris: IPH; Nasdaq: IPHA) (“Inna...

STAT+: Trump administration to fire thousands at health...

The Trump administration is set to eliminate thousands of federal health care jo...

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