At the 2025 Veeva Commercial Summit Europe, experts touted the benefits of AI but stressed the importance of data and ...

Made Scientific and Cellergy Therapeutics have formed a partnership to advance CLG-001 mitochondrial therapy towards in-human ...

Novartis has received approval from the US Food and Drug Administration (FDA) for the Itvisma gene replacement therapy to ...

Lilly breaking through the $1tn market cap ceiling comes as investors have increasingly turned to pharma stocks. The S&P 500 ...

While the Phase III results confirm prior analyst sentiments, a KOL notes that GLP-1RAs could still show potential in the ...

An FDA officer explains the agency’s compliance requirements for importing pharmaceuticals and biologics and processes.

In 2024, the FDA granted a record 63 designations to antibody drug conjugates (ADCs), nearly double the previous high of 35 ...

The industry is showing enthusiasm for novel technologies that improve safety and carry innovation potential including in vivo CAR-Ts.

Advances in large-volume injectors are enabling faster, more comfortable, at-home treatment. Patient-centric design, ...

OSR Company Vaximm has linked with investor BCM Europe (BCME) for a potential exclusive worldwide licence for Vaximm’s VXM01.

Roche has received conditional marketing authorisation from the European Commission (EC) for Lunsumio (mosunetuzumab) ...

Pfizer and Tris Pharma have agreed to pay $41.5m to settle allegations by Texas Attorney General Ken Paxton that they ...