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- Configured to meet the requirements for USP <467> including column, consumables, calibration/checkout samples, and analytical method, which facilitates adaptation to your laboratory SOPs
- GC/MS/FID analysis provides identification and confirmation of organic contaminants in pharmaceutical active ingredients, formulations, and additives
- Headspace thermal zone stability of ± 0.1 °C, inert flow path, and use of patented capillary flow technology (CFT) provides ≤ 3% for USP Class 1A and Class 2A/B solvents
- Pre-configured per industry standards and chemically tested ensuring optimal analysis of Class 1 and Class 2A/B solvents in pharmaceutical products
- Includes CD-ROM with optimized acquisition method for residual solvent analysis, and quick start guide for faster method validation
- On-site installation and check out by a factory-certified technician confirm that your instrument and application meet Agilent analytical performance criteria
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