_data-integrity-for-infrared-and-raman-spectroscopy-in-opus.jpg "Data Integrity for infrared and Raman spectroscopy in OPUS from us fda cfr 21 Video Screenshot Preview")
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⏲ Duration: 9 min 68 sec
✓ Published: 28-May-2018
✓ Published: 28-May-2018
Description:
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
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
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