EMEA Office
Kantersteen 47
1000 Brussels
Belgium
Dec 1, 2026 11:00 AM (CET)
Repeat deviations and audit findings rarely come out of nowhere. The warning signs are often already in your quality data: overdue CAPAs, recurring minor deviations, or persistent training gaps. But when the focus is on closing records, the bigger picture gets missed.
In this CaseLab, Milind Nadgouda, Co-founder & Director of Operations at RiverArk, uses a real, anonymized GMP case to show how overlooked signals can escalate into audit findings, and how to spot patterns early by combining data with context.
Christopher Hayden, Partnership Manager at Scilife, will then demonstrate how a modern eQMS connects events, CAPAs, and training data to help teams identify risks and act before they become findings.
You’ll leave with:
Milind Nadgouda is a QA leader with more than 30 years of strategic and operational experience across the pharmaceutical and life-sciences sectors. His expertise covers GxP inspection readiness, audit strategy, quality-risk management and regulatory compliance. He has supported major pharmaceutical organisations both on the frontline and behind the scenes during regulatory inspections.
Christopher Hayden is Head of Partnerships at Scilife, with a background in business development and science. He works closely with consulting firms and industry experts to grow Scilife’s global partner network, helping life sciences companies simplify compliance, strengthen quality processes and accelerate their digital transformation.
EMEA Office
Kantersteen 47
1000 Brussels
Belgium
US Office
Scilife Inc.
228 E 45th St. RM 9E
New York, NY 10017
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EMEA Office
Kantersteen 47
1000 Brussels
Belgium
US Office
Scilife Inc.
228 E 45th St. RM 9E
New York, NY 10017
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