Data Integrity for infrared and Raman spectroscopy in OPUS from us fda cfr 21 Watch Video
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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
Play Video: (Note: The default playback of the video is HD VERSION. If your browser is buffering the video slowly, please play the REGULAR MP4 VERSION or Open The Video below for better experience. Thank you!)