Valkit MSAT digitizes GxP tech transfer with global package cloning, CDMO isolation, paperless execution, and a fixed ...

Legacy revenue management systems excel as auditable systems of record but fail on novel structures, forcing Excel ...

Discover how quality-driven drug development and AI accelerate safer medicines, reduce risk, and improve patient outcomes.

The integration of process models into pharmaceutical manufacturing has gained considerable attention in recent years due to their potential to enhance efficiency, productivity, and quality control.

Pharma companies in the UK are being invited to register their new medicines with both the MHRA and NICE at the same time, as part of a push to reduce regulatory review times by three to six months.

Zifo, a premier global provider of AI and data-driven informatics for science-focused organizations, today announced the ...

Advanced hybrid AI approach combines OCR and Large Language Models to transform manual document processing into real-time digital insights.CAMBRIDGE, Mass. and CAMBRIDGE, England, April 28, ...

In April 2023, the European Commission published its pharma package and on 4 June 2025 the Council agreed its negotiating position (mandate). On 11 December 2025 the Council and the Parliament reached ...

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Regulatory approval is a major milestone in the drug development process, but it is not the final chapter in the journey.

Blood flows through the blood vessels to deliver the needed oxygen and nutrients to the different cells in the body. The blood clotting process or coagulation is an important process that prevents ...

Barbara Slusher explains the hit-to-lead optimization process, high-throughput screening, and the role of AI and organoids in ...