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Using the Cary 630 FTIR spectrometer and Agilent MicroLab FTIR software to perform fast, easy, and reliable workflows for the analysis of different sample-types.
The use of the Cary 630 FTIR for analyzing polymers used in pharmaceutical packaging.
| Chinese (Simplified) (China) | Complete (PDF) |
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SDA Compliance for Agilent ICP-MS Systems
Meeting the requirements of the global pharmacopeias with the Agilent Cary 3500 UV-Vis
| Chinese (Simplified) (China) | Complete (PDF) |
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| Japanese (Japan) | Complete (PDF) |
| Korean (Korea) | Complete (PDF) |
Demonstrates simple and fast sample submission with the Agilent InfinityLab LC/MSD iQ for multiple users utilizing the sample purity workflow in an open-access environment.
| Russian (Russia) | Complete (PDF) |
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| Japanese (Japan) | Complete (PDF) |
| Korean (Korea) | Complete (PDF) |
| Chinese (Simplified) (China) | Complete (PDF) |
Separation and purification of acetaminophen (paracetamol) and six common impurities listed in the EP and USP.
Solid-phase micro-extraction (SPME) and GC/MS/MS method for graftage-related black tea samples with data extraction and analysis via MH Profinder and MPP
| Korean (Korea) | Complete (PDF) |
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The application note describes a nontarget modification-specific metabolomics approach to study glycosylation modifications in various types of tea plants.
This application note describes statistical analysis and identification of extractables and leachables from ophthalmic drug products
Software-based data interpretation greatly alleviates the challenge of data interpretation and compound identification in extractable and leachable study.
Details of how these products support compliance with electronic signature regulations
| Korean (Korea) | Complete (PDF) |
|---|---|
| Chinese (Simplified) (China) | Complete (PDF) |
| Japanese (Japan) | Complete (PDF) |
| Russian (Russia) | Complete (PDF) |
Expanded support for USP / and ICH Q3D methods supports compliance with elemental impurity analysis in pharmaceutical materials via ICP-OES
The cloud has become a viable option for virtually every computing workload in the laboratory, from sample management to complex analytics to secure data storage. This white paper gives lab managers fresh insights into multiple aspects of cloud...
| Russian (Russia) | Complete (PDF) |
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This executive summary explores what the paradigm shift in regulatory audits means for analytical laboratories, the FDA’s goals during an inspection, systems that could be subject to inspection, mechanisms to ensure data integrity in analytical...
The article provides a foundation for thinking about software validation based on expert articles and US FDA resources and consultants.