Spectroscopy Solutions for Pharmaceuticals

Technické články | 2016 | Agilent TechnologiesInstrumentace
UV–VIS Spektrofotometrie
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Farmaceutická analýza
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Agilent Technologies
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UV-VISIBLE HARDWARE OPERATIONAL QUALIFICATION
2012|Agilent Technologies|Ostatní
UV-VISIBLE HARDWAREOPERATIONAL QUALIFICATIONAgilent Enterprise Edition Compliance ServicesStandard OQ Test Specifications for UV-Visible SpectrophotometersThe following tables describe the core hardware testing specifications for UV-Visible systems. See the correspondingattachment for a description of the optional tests available for UV-Visible systems, not part...
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Application NotePharmaceutical Analysis UsingUV-Vis: Compliance with USP Chapter<857>, and European Pharmacopoeia(Ph. Eur. Chapter 2.2.25)Meeting the requirements of the globalpharmacopeias with the Agilent Cary 3500 UV-VisIntroductionUV-Vis spectroscopy is a widely used analytical technique in quality assurance/quality control (QA/QC) and pharmaceutical research....
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White PaperPharmaceutical Analysis usingUV-Vis: Compliance withSupplement I to the JapanesePharmacopoeia 18th Ed., Section 2.24Meeting the requirements of the globalpharmacopeias with the Cary 3500 UV-VisIntroductionUV-Vis spectroscopy is a widely used analytical technique in quality assurance/quality control (QA/QC) and pharmaceutical research. It...
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USP General Chapter <857> andPh. Eur. Chapter 2.2.25 10th EditionMeeting requirements with the Cary 60 andCary 3500 UV-Vis spectrophotometersQualification of instrumentsUpdates to the United States Pharmacopeia (USP) General Chapter <857>and the European Pharmacopoeia (Ph. Eur.) Chapter 2.2.25 will requiresome changes...
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