---
title: [Webinar] USP <87> Biological Reactivity Testing
description: "Attend this webinar, USP <87> Biological Reactivity Testing: Future-Proofing Your Strategy, presented by an expert at Pace® Life Sciences."
---
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# USP \<87\> Biological Reactivity Testing: Future-Proofing Your Strategy
The pending December 1, 2026 update to USP \<87\> marks a decisive industry shift toward modern, science-based in vitro testing and quantitative risk assessment for pharmaceutical and medical device manufacturing. Navigating these regulatory updates requires a proactive strategy to evaluate material qualification, biological evaluation, and laboratory planning long before mandatory enforcement. Modernizing testing frameworks early prevents operational bottlenecks, minimizes reliance on legacy protocols, and aligns compliance strategies with evolving global standards. Exploring anticipated structural changes, validation impacts, and proactive readiness steps allows organizations to safeguard product development timelines while enhancing testing precision.
Access the full webinar to gain expert insights on structuring a future-proof biological reactivity compliance framework.
*Originally released with Outsourced Pharma*
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**Jillian Miller, Microbiology Manager**
**Pace® Life Sciences – Lebanon, NJ**
Jillian Miller is a Microbiology Manager at Pace® Life Sciences with more than 15 years of experience of experience in the industry. She joined Pace® following the company's acquisition of the Curia’s Lebanon, NJ site, formerly known as Whitehouse Analytical, where she served as Department Head of Microbiology for nearly eight years. Jillian specializes in microbiological testing, laboratory operations, and regulatory compliance, helping pharmaceutical and biopharmaceutical companies navigate evolving compendial requirements. She holds a B.S. in Biology from Salisbury University.
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