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Medical Device Academy
Medical Device Academy
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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")
_us-fda-21-cfr-overview.webp "Learn gmp Inc.")
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_what-is-fda-cfr-21.webp "Medical Device Training")
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