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Demystifying Software Validation: Learn What Software Validation Means for You and Your Lab

 

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Data Integrity in Pharmaceutical Quality Control Laboratories: What You Need to Know Whitepaper Author Loren Smith, Agilent Technologies, Inc. Santa Clara, CA USA Data integrity problems in pharmaceutical quality control laboratories are driving more regulatory action than ever before. What…
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White Paper Support for 21 CFR Part 11 and Annex 11 Compliance: SDA Module for Agilent ICP-MS MassHunter Software Overview Part 11 in Title 21 of the US Code of Federal Regulations (commonly referred to as 21 CFR Part 11)…
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White Paper Meeting Regulatory Compliance Guidelines with Agilent ICP-MS MassHunter and OpenLab Server or ECM XT Overview The United States Pharmacopoeia (USP) and the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) are responsible for…
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The NanoRam Hand-held Raman Spectrometer: Full Regulatory Compliance for the Inspection of Raw Materials and Chemicals Used in the Pharmaceutical Industry One of the most critical factors in developing and marketing pharmaceutical drug products and dietary supplements today is ensuring…
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