Discussion forum for Pharma Quality events, Regulatory Actions
Warning letters, 483s, Recalls, Import Alerts, Audit observations
Warning letters, 483s, Recalls, Import Alerts, Audit observations
A panel of Pharma domain experts guide and suport Qvents. The Qvents Expert Panel have diverse and rich experience across Pharma Technical Operations – Quality, Regulatory, R&D, Manufacturing, Engineering, Audits, Remediations, IT Enhancement.
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