Enhancing biopharma workflows with the power of UV/Vis spectroscopy

Technology5/15/2024 3:00 PM

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Discover the valuable role ultraviolet-visible spectroscopy can play in quickly and accurately monitoring a drug as it moves through the research & development workflow and enabling quality and regulatory compliance through the manufacturing process. This webinar will explore nucleic acid sample quality, the use of spectrophotometric analysis, tips for ensuring compliance with the 21 CFR Part 11 regulation, and more.


Justin Shaffer, Product Marketing Specialist, Thermo Fisher Scientific


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European Pharmaceutical Review

European Pharmaceutical Review

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