Past Webinar
Enhancing biopharma workflows with the power of UV/Vis spectroscopy
Technology5/15/2024 3:00 PM
Description
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.
Speakers:
Justin Shaffer, Product Marketing Specialist, Thermo Fisher Scientific
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Publisher
European Pharmaceutical Review is a leading source of information for the pharmaceutical industry. They provide news, articles, podcasts, webinars, and other content related to various topics in the pharmaceutical field such as analytical techniques, biopharma, drug delivery, formulation, manufacturing, packaging, quality assurance, research and development, regulations, and legislation. Stay up to date with the latest trends and developments in the pharmaceutical industry by following European Pharmaceutical Review.