
At ISC 2026, a 20-minute IP-RPLC–UV assay distinguished mRNA capping variants without mass spectrometry, matching a UHPLC–MS reference method.
The two questions to ask when considering the validation of computerized laboratory systems are "Do I need to validate the system?" and,if so,"How much work do I need to do?" This article provides a simple framework to answer these questions at the system level.
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Analytical Instrument Qualificationabout 20 years ago
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Team Effortabout 20 years ago
Rated PG: Pharmaceutical Guidance Suggestedabout 20 years ago
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FDA Video Interview Conducted by Jill Wechsler, Washington Bureau Chiefabout 20 years ago
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2006: A Regulatory Odysseyabout 20 years ago
CDER?s Division of Post-Marketing Evaluation for Quality Assessment