Lilly licenses Insilico's AI drug discovery platform in a deal worth up to $2.75B, signaling a shift in how novel ...
The 2023 revision of Annex 1 of the European Union’s good manufacturing practice (GMP) guidelines 1 represents a fundamental shift in expectations for sterile manufacturing. Reg ...
Using patent intelligence data from the FounderNest platform, alongside funding, partnership, and deployment signals across ...
During its March 2026 meeting, the agency’s Committee for Medicinal Products for Human Use approved treatments for Bacillus ...
EMA approved Johnson & Johnson’s daratumumab SC for self-administration, Europe’s first oncology injectable to offer this ...
Scale-up involves increasing pump sizes, reactor volumes, and flow rates—but the process control logic and system ...
The FDA has approved a high-dose regimen of Biogen’s nusinersen (SPINRAZA) for the treatment of spinal muscular atrophy. 1 ...
Michelle Dennis, QC Microbiology Application Specialist with MilliporeSigma and member of the PDA Week 2026 planning ...
Ryan Murray, ValSource, breaks down far UVC technology, holistic contamination control strategies, and environmental ...
In this insightful interview, Richard Jaenisch, senior director of Education, Outreach, and Digital Experience at Open ...
Malav Parikh, director, Quality Risk Management, Global Quality Compliance and Systems, Takeda, spoke with PharmTech about ...
By incorporating these advanced models into preclinical packages for the FDA, researchers can provide a much stronger proof ...
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