The company will highlight how its GMP services combine engineering, consulting, equipment qualification, and facility ...

Dave Miller, PhD, explains how early formulation planning, novel platforms, and tailored approaches secure long-term protection against generics.

Based on an analysis done by the European Medicines Agency on the feasibility of alternatives, the European Commission ...

Dave Miller, PhD, discusses how shifting drug manufacturing to domestic CDMOs can improve quality, reduce rework, and enhance ...

The company’s commitment to its North Chicago, Ill. plant is part of a previously announced $10 billion capital investment ...

For the first target addressed in the partnership, the two companies reported the successful delivery of AI-designed, ...

The new targeted pipeline will advance Nxera’s oral GLP-1 agonists, novel GPCR targets, and structure-based drug design to ...

Experts from LGM Pharma and Rockwell Automation share their thoughts on what makes tech transfer effective, where processes ...

The scaled adoption of cell and gene therapies demands a new era of agile, precise, and efficient quality control methods.

The agency’s new program is designed to increase regulatory predictability and streamline review of domestic manufacturing ...

Dave Miller, PhD, explains how environmental audits, waste reduction, and supply chain security are reshaping priorities in pharmaceutical manufacturing.

Jerry Keybl, senior vice-president, Biopharma Products and Strategy, Avantor, discusses innovations in biomanufacturing and ...