Dec 01, 2017
BioPharm International
Cross-functional reliability rooms identify risk and planning metrics, provide insights for production forecasts, and predict trends and areas for improvement.
Dec 01, 2017
BioPharm International
The Biomanufacturing Technology Roadmap is accelerating innovative manufacturing strategies for biopharmaceuticals.
Dec 01, 2017
BioPharm International
A roundtable Q&A with biopharma executives elucidates the challenges posed by single-use bioreactor bags in contributing to extractables and leachables in the biomanufacturing process.
Dec 01, 2017
BioPharm International
A quality-by-design approach that implements PAT offers advantages in upstream cell-culture processing.
Dec 01, 2017
BioPharm International
A technology roadmap aims to drive and consolidate improvements in a process that has remained unchanged for more than 70 years.
Dec 01, 2017
BioPharm International
Developing and retaining qualified employees will test biopharma companies and CMOs alike.
Dec 01, 2017
BioPharm International
Single-use systems provide replaceable fluid paths.
Dec 01, 2017
BioPharm International
Biopharma employees reveal employment objectives, opportunities, and frustrations.
Dec 01, 2017
BioPharm International
SOPs need to reflect a company’s specific manufacturing or other operations, says Susan Schniepp, distinguished fellow at Regulatory Compliance Associates.
Dec 01, 2017
BioPharm International
In a productive year, 2017 was filled with acquisitions, facility expansions, and new biopharma technology.
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