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LC/MS based characterization workflow of the GLP-1 therapeutic peptide liraglutide and its impurities using the 1290 Infinity II LC and 6545XT AdvanceBio LC/Q-TOF.
必威体育登录手机Agilent Atomic Absorption Spectrometers deliver high performance that analysts require while being equally at home in routine labs where reliabiltiy is vital.
必威体育登录手机Agilent Vaya handheld Raman spectrometer with SORS can identify hazardous materials in original packaging, ensuring worker-safety.
State-of-the-art solutions for oligonucleotide characterization, purification, and manufacturing.LabX eBook.
必威体育登录手机This application note demonstrates the use of the Agilent 8890 GC system coupled with an FID detector to detect and quantify ethylene glycol and diethylene glycol in propylene glycol, glycerin and syrup samples.
必威体育赛事投注FTIR and chemometrics were used to determine the potency of several forms of cannabis products.
必威体育登录手机This application note describes the opaque container analysis capabilities of the Agilent Vaya handheld Raman spectrometer.The discussion focuses on identity verification of common excipients and APIs through blue drums.
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| Japanese (Japan) | Complete (PDF) |
| Chinese (Simplified) (China) | Complete (PDF) |
必威体育登录手机Agilent Vaya handheld Raman spectrometer with SORS can identify metal stearates in original packaging, without the need for complex chemometric software packages.
| Chinese (Simplified) (China) | Complete (PDF) |
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| Korean (Korea) | Complete (PDF) |
| Japanese (Japan) | Complete (PDF) |
Learn about proven workflows for regulatory compliance, enhance drug quality and safety, simplify analysis with cutting-edge technology.
必威体育登录手机Compares Analytical Instrument Qualification using Agilent ACE with other options using Data Integrity and compliance with USP general chapter as a framework.
This application note describes the validation of a procedure for the measurement of elemental impurities in sterile artificial tear eye drops (SATED).
必威体育登录手机The Agilent workflow solution for implementing an elemental impurities analysis capability in compliance with USP / and ICH Q3D.
Reducing the time and expense of ICP-MS method development and system validation for measuring elemental impurities in pharmaceuticals
Learn how to save solvent and analysis time when transferring methods to UHPLC conditions in accordance with USP Chapter requirements.
| Japanese (Japan) | Complete (PDF) |
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| Chinese (Simplified) (China) | Complete (PDF) |
必威体育登录手机The original United States Pharmacopeia (USP) monograph HPLC methods for assay and related compounds analysis of insulin and human insulin were modernized with Agilent InfinityLab Poroshell 120 columns following the newly revised USP guidelines.
| Japanese (Japan) | Complete (PDF) |
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| Chinese (Simplified) (China) | Complete (PDF) |
This application note demonstrates the benefits of combining helium collision mode and discrete sampling to develop and validate an easy-to-use, polyatomic interference-free method for the determination of 13 elements in tea infusion.
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In this application note, the Vaya handheld Raman spectrometer's discrimination capability through opaque and transparent containers is described for closely related raw materials like sugars, fatty acids, glycols, diols, and other common...
必威体育赛事投注Details of how these products support compliance with electronic signature regulations
| Chinese (Simplified) (China) | Complete (PDF) |
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| Korean (Korea) | Complete (PDF) |
必威体育登录手机In this study, an analytical workflow was developed in accordance with the ICH/USP guidelines for the analysis of elemental impurities in an oligonucleotide sample using an Agilent 7850 ICP-MS.
New limits for elemental impurities in pharmaceutical materials and dietary supplements have been released by the USP and ICH.