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Your laboratory equipment lacked sufficient controls to prevent and detect deletion or manipulation of your laboratory's electronic raw data." 8 Detailed Analysis of the Violation Spectroscopy Audit Trails: The FDA noted that "ultraviolet-visible (UV-vis) and infrared (IR) spectroscopy equipment was found to lack audit-trail functionality".8 Historically, regulatory focus has been on HPLC and GC data

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Journal of the American Chemical Society

Transgenic mouse models of Alzheimer disease: developing a better model as a tool for therapeutic interventions