Prepare for the December 1, 2026 release of revised USP <87>. Join Pace® Life Sciences for a webinar exploring anticipated changes to in vitro biological reactivity testing, evolving regulatory expectations, and practical preparation strategies. Experts will discuss impacts on material qualification, validation, compliance, and operational efficiency across testing programs today. Click here to learn more.
Build a secure, scalable bridge between shop-floor systems and enterprise IT with an interoperable integration strategy designed for today's manufacturing needs and tomorrow's growth.
Bridge the gap between your production floor and quality governance. Discover how a unified QMS and MES platform eliminates paper records, automates deviation triggers, and utilizes secure AI tools.
Digitizing shop-floor operations improves accuracy, accelerates workflows, and strengthens compliance. See how real-time data capture, automated processes, and unified visibility help teams reduce risk.
Upgrade your compliance strategy with accredited, scenario-based GxP training. Eliminate risks like failed inspections and costly deviations with a modern, global solution.
Access FMS Anywhere! OPC UA Client/Server functionality to monitor particle counts and other environmental parameters—makes great business sense in order to reduce waste, improve yield, improve quality and increase profits.
Automated washing of 3D spheroids improves consistency, reduces cell loss, and streamlines staining workflows. See how this approach enhances reproducibility and throughput in microplate-based assays.
When it comes to solid dosage formulations, the most common challenge formulators face is poor solubility. In numbers: 70% of drugs in development are poorly soluble.
Pharmaceutical Online, Federal Equipment and Techceuticals bring you Virtual Pharma Expo - a themed event featuring presentations by leading experts from pharmaceutical equipment providers for oral solid dose manufacturing and packaging.
