Industry subject matter experts spoke about the challenges of turning complex molecules into medicines patients can reliably use.
|Articles|February 2, 2018
- Pharmaceutical Technology-02-02-2018
- Volume 42
- Issue 2
Pharmaceutical Technology, February 2018 Issue (PDF)
Click the title above to open the Pharmaceutical Technology February 2018 issue in an interactive PDF format.
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Articles in this issue
almost 9 years ago
Designing a Single-Use Biopharmaceutical Processalmost 9 years ago
Material Traceability in Continuous Pharmaceutical Tablet Manufacturingalmost 9 years ago
Analyzing Content Uniformityalmost 9 years ago
Impurity Testingalmost 9 years ago
Tabletop Peristaltic Liquid-Filling Machinealmost 9 years ago
Safety Light Curtain Feature on Tumble Blendersalmost 9 years ago
Aqueous Sugar Film Coating Systemalmost 9 years ago
USB Data Logger for Temperature-Sensitive ProductsAdvertisement
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The pharmaceutical supply chain is a complex system with high stakes. USP provides insights on how it is helping industry navigate global disruptions and procurement issues.
Jaenisch, Muraru, and Pandey discuss how regulators will audit pharma against its own AI policies and ways QA and regulatory teams can build defensible, inspection-ready AI practices.
Impurity deficiencies in submissions are remarkably consistent. Subathra Ramamoorthy, Veranova, explains how to catch them before agency filing.
USP’s Sheehan and Liu talk at AAPS PharmSci 360 abou getting novel excipients past the monograph hurdle through early engagement with FDA.
CDMOs announced expansions, exhibitors showcased automated equipment, and supply chain strategy discussions were a focus at CPHI Milan 2026.
Mitigating nitrosamine risk requires assessing each product individually and chasing zero nitrite in pharmaceutical excipients is often impractical and costly.
The business case for regulated AI turns on the cost of producing an outcome that the quality system can accept.
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