Newsletter | May 30, 2024

05.30.24 -- 7 Bioprocess Intensification Strategies

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Webinar: Measuring Viral Vector Purity, Stability, and Physical Titer in Minutes — with Just One Tool

Industry expert Dr. Laura Pala will highlight the advantages of macro mass photometry to characterize viral vector purity and stability, and help you understand how the KaritroMP can quickly assess the purity of AdV preparations, quantifying empty capsids and other impurities. Click here to learn more.

FOCUS ON ANALYTICS & QUALITY

7 Bioprocess Intensification Strategies

By Matthew Pillar, Editor, Bioprocess Online

“Process intensification” is one of those umbrella terms that unfairly implies a concept that comes with instructions. It doesn’t. It isn’t prescriptive. It doesn’t have to start in a specific place, and it never ends.

Imagine The Future: Enhanced Oligonucleotide Synthesis

Article | By Lucy Cook, Ph.D., Cytiva

Learn about flexible control software that has revolutionized the way method creation, evaluation, and process optimizations for scale-up are completed.

Three Ways Manufacturing Excellence Drives Value For Life Sciences

Article | By Shawn Opatka, Honeywell Process Solutions

Check out three ways Honeywell’s Manufacturing Excellence Platform delivers value in terms of costs, revenue, and risk.

ANALYTICS & QUALITY SOLUTIONS

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The Industrial DataOps Solution For Industry 4.0 - HighByte

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Power Your Process Development Digital Data Strategy - IDBS UK HQ

FOCUS ON REGULATORY

Navigating Grades And Sources Of Materials In Drug Manufacturing

By Allison Radwick, RPh, Ph.D., U.S. Pharmacopeia

From raw materials to finished dosage forms, understanding material quality is essential in drug manufacturing. This article examines how material grades and sources guide selection for optimal safety and functionality.

Developing A Comprehensive Regulatory Approach For LNP Drugs

Article | Precision NanoSystems

The path to regulatory approval for LNPs demands carefully considered strategies. By adopting proactive and strategic approaches, developers can overcome regulatory hurdles on the path to approval.

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