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Biotech Organization Partners with Advarra to Become Inspection Ready
An established biotech organization sought out a partner to provide investigator site audits, trial master file (TMF) audits, for-cause audits, and other quality assurance services. Turning to Advarra, they developed a partnership through Advarra’s proven GxP services and successful U.S. Food and Drug Administration (FDA) guidance.
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Time: 1 p.m. ET, 12 p.m. CT, 10 a.m. PT
Duration: 1 hour