Process validation is crucial for ensuring the quality of final products and the safety of these processes for manufacturing personnel and consumers in the pharmaceutical, medical device, and ...

In pharmaceutical manufacturing, cleaning validation is an essential stage of verifying that the manufacturing process is suitable. As an integral stage of the cleaning validation program, analytical ...

Data integrity is key to the success of any cell therapy program. CDMOs can implement robust data management systems for ...

The pharmaceutical manufacturing software market offers growth opportunities through increased regulatory compliance and the ...

USP is developing digital reference standards to integrate into modern digital environments, enhancing regulatory confidence ...

In biopharmaceutical manufacturing, consistency is vital but hard to achieve. Turning raw materials into safe, high-quality medicines requires stable processes. However, the living cellular expression ...

This week's report explores the pharmaceutical industry’s evolution toward resilient, scalable systems that prioritize ...

Quantumzyme Corp. (OTC: QTZM), a biotransformation company focused on sustainable pharmaceutical manufacturing, today announced a breakthrough advancement in its proprietary enzyme development ...

BOCA RATON, Fla.--(BUSINESS WIRE)--LGM Pharma, a leading provider of tailored API and CDMO services for the full drug product lifecycle, today announced a significant enhancement of its capabilities: ...

Shibuya Corporation's systems include integrated isolators, sterilization technologies, and filling solutions that deliver ...