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Pharma Quality
Pharma Quality
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_gxp-in-pharmaceuticals.webp "Pharmaguideline")
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_data-integrity-for-infrared-and-raman-spectroscopy-in-opus.webp "Pharmaceutical industries face extensive regulations by authorities. For GMP or any other Good Practices (GxP) the FDA described the handling of electronic data with 21 CFR part 11.nTo support our customers Bruker provides a spectroscopic software that assures that all requirements for full compliance are met.nnhttps://www.bruker.com/products/infrared-near-infrared-and-raman-spectroscopy/opus-spectroscopy-software/base-package/validation.html)nnStandard OPUS validation functions:nn- Extensive pa")
_computer-system-validation-in-pharmaceutical.webp "GMP-SOP Videos")
_how-to-modernize-gxp-training-by-unifying-quality-systems.webp "Veeva Systems Inc")
_sop-management-system-demonstration.webp "Standard Operating Procedures (SOPs) are essential to all quality-related, GxP compliant processes as well as the ability to verify that employees are being trained on these SOPs appropriately. SOPs must be well organized, up-to-date, reviewed and approved in a defined schedule, and modified with documentation. Additionally, enterprise-wide training programs must include automated methods for new employee on boarding, and for annual refresher training.")
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