Recent posts

Webinar Recap: “Developing, Testing, and Troubleshooting Chromatography Method Transfer”

By February 1, 2017

In this webinar, we discussed the transfer of chromatographic methods that occurs at many stages in the development and production of a product. Here are a few questions that we received but did not have time to answer during the information-rich hour.

Categories: Technologies
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The Waters ACQUITY Arc System Receives 2016 Frost & Sullivan New Product Innovation Award

By October 4, 2016

Bridging the gap between HPLC and UPLC performance, the ACQUITY Arc System is a favorite of QC laboratories that test small and large molecule pharmaceuticals. We’re excited to announce today (Tuesday, Oct. 5) that our… Read more >

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Out with the old, in with the new…

By May 3, 2016

We’re all familiar with the adage, “Out with the old, in with the new,” but we probably tend to think of it as it applies to clothes for donation or past relationships, and maybe not… Read more >

Categories: Pharmaceutical
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ACQUITY Arc System: Transferring Validated HPLC Methods within USP Guidelines

By March 8, 2016

The thought of transferring established high performance liquid chromatography (HPLC) methods onto a another vendor’s LC, or a new platform like UHPLC/UPLC, may cause a bit of anxiety for those that may be unaware of… Read more >

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Unleash the maximum separation performance from your solid-core column

By December 3, 2015

Webinar Highlights | Understanding the Impact of System Dispersion on Separation Performance Hi, I am Jonathan E. Turner, Product Marketing Manager for ACQUITY® UPLC® and CORTECS® lines of columns at Waters Corporation. I recently conducted… Read more >

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Attention Method Development Scientists! Learn about novel tools for replicating your existing methods

By November 18, 2015

Webinar Highlights | Simplifying Methods Transfer: Novel Tools for Replicating Your Established Methods on an ACQUITY Arc System I’m Dr. Paula Hong, Principal Scientist at Waters Corporation. I recently conducted a webinar that talked about the… Read more >

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Dispersion Matters: Rethinking How LC Systems Should be Categorized

By June 19, 2015

For more than five decades, attempts have been made to improve liquid chromatography separations performance by reducing the particle size of the stationary phase. However, the benefits of doing so can only be realized if… Read more >

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Chapter and Verse: USP 621 and You

By February 23, 2015

In August 2014, the United States Pharmacopeia and the National Formulary (USP-NF) put into effect new guidelines to “allowable adjustments” in its Chapter <621> (USP37-NF32 S1). And as of August 1, 2016 when USP 39… Read more >

Categories: General, Pharmaceutical, Technologies
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Webinar discusses new purity method, 40X increase in productivity

By October 30, 2014

Webinar: QbD Development of a Purity Method Chromicent GmbH (Berlin, Germany) managing directors Alexander Schmidt and Mijo Stanic are experts in the development and validation of analytical methods according to the latest quality-by-design approaches. The… Read more >

Categories: Pharmaceutical
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