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Pharmacopeial Modernization: How Will Your Chromatography Workflow Benefit?

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Register for a free SelectScience webinar to learn more about the pharmacopeial monograph modernization prioritization scheme

12 Sept 2018
Sarah Thomas
Associate Editor

Expert insights

Experts from the United States Pharmacopeia and Waters will discuss pharmacopeial modernization

In an upcoming webinar, Dr. Leonel Santos and Dr. Horacio Pappa from the United States Pharmacopeia (USP) will provide an overview of its pharmacopeial harmonization and modernization efforts.

The pair will also review changes described in the pending USP General Chapter <621> on chromatography, which will provide increased flexibility for gradient methods.

Amanda Dlugasch, from Waters Corporation, will follow with an illuminating case study, which leverages USP <621> allowable adjustments to illustrate the benefits of modernizing methods without the need to revalidate.

Register now

Topics explored will include:

  • The pharmacopeial monograph modernization prioritization scheme
  • A review of USP General Chapter <621> current allowable adjustments to validated methods and forthcoming updates
  • A case study on the migration of isocratic and gradient pharmacopeial methods to modern column technology, highlighting improved method performance and throughput

Attend the live webinar on Thursday, September 27, at:

  • 15:00 BST
  • 16:00 CEST
  • 10:00 EDT
  • 07:00 PDT

Interested, but have a scheduling conflict? Register to receive an on-demand link to watch later.

SelectScience runs 3-4 webinars a month across various scientific topics, discover more of our upcoming webinars or watch our past webinars on demand>>

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UHPLC and HPLCHigh performance liquid chromatography (HPLC) and ultra high performance liquid chromatography (UHPLC), also known as UPLC, are analytical techniques used to separate, identify and quantitate components of complex mixtures including biological samples such as proteins and lipids as well as chemical mixtures of pesticides, drugs and oils. Both techniques are liquid chromatographic methods but differ by operating pressures (HPLC < 6000 psi < UHPLC ). Components of HPLC and UHPLC systems include columns, detectors, pumps, autosamplers and column heaters. Explore a range of UHPLC and HPLC columns for your specific sample needs including reverse phase, normal phase, ion exchange, HILIC, ion exclusion and size exclusion columns. For more specialized HPLC, explore FPLC, countercurrent LC and simulated moving bed systems. Find the best UHPLC and HPLC equipment in our peer reviewed product directory: compare products, check customer reviews and receive pricing direct from manufacturers.Chromatography Method DevelopmentChromatography method development is the process of designing and optimizing chromatographic techniques to separate and analyze complex mixtures. This includes selecting appropriate stationary and mobile phases, determining flow rates, and optimizing detection methods. Successful method development is essential for high-quality results in fields like pharmaceuticals, food safety, and environmental analysis. Explore chromatography method development tools in our peer-reviewed product directory; compare products, check reviews, and get pricing directly from manufacturers.ChromatographyChromatography is a powerful technique used to separate and analyze components of mixtures based on their chemical properties. It is widely used in fields like biochemistry, pharmaceuticals, and environmental analysis. By exploiting differences in the interaction of substances with a stationary phase and a mobile phase, chromatography enables precise purification and quantification of compounds. Whether you're working with complex biological samples or industrial chemicals, chromatography is essential for obtaining high-quality results. Browse our peer-reviewed product directory to find the best chromatography systems, compare products, read customer reviews, and get pricing directly from manufacturers.Method ValidationMethod validation is the process used to prove that the analytical procedure used for a particular test is capable of providing suitable data.USP Method

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