Why Laboratory Compliance is Essential to Valid Analytical Results
Brožury a specifikace | 2020 | Agilent TechnologiesInstrumentaceZaměření
Farmaceutická analýza
VýrobceAgilent Technologies
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Regulatory 101. What is AIQ? Complete DQ/IQ
2015|Agilent Technologies|Prezentace
Regulatory 101 What is AIQ ? Complete DQ/IQ Paul Smith Global Strategic Compliance Program Manager Agilent Technologies, Inc. July 9, 2015 Confidentiality Label July 10, 2015 1 10 Steps to a “New Instrument”…. User Requirement Specification URS 1. • •…
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Agilent Equipment Qualification Solutions
2020|Agilent Technologies|Brožury a specifikace
Agilent Equipment Qualification Solutions Qualify the Instruments in Your Laboratory with a Harmonized, and Data Integrity Compliant Solution Instrument Qualification – A Regulatory Requirement For your analytical results to be valid, your analytical instruments must be suitable for their intended…
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Recommendations for Hemp Testing: Laboratory Compliance
2021|Agilent Technologies|Technické články
Technical Overview Recommendations for Hemp Testing: Laboratory Compliance Author Matthew Abrahms Agilent Technologies, Inc. Abstract Designed as a follow-up to the Agilent United States Hemp Testing white paper,1 this technical overview presents recommendations to the industry on laboratory compliance. These…
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Analytical Instrument Qualification with Data Integrity in Mind
2022|Waters|Technické články
[ ARTICLE ] Analytical Instrument Qualification with Data Integrity in Mind Heather Longden, Senior Marketing Manager, Pharmaceutical Regulatory Compliance Waters Corporation, Milford, MA, USA It is critical to understand the data integrity implications regarding analytical instrument qualification. OVERVIEW Analytical Instrument…
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