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.
QA Specialist
Lorem Ipsum is simply dummy text of the printing and typesetting industry. Lorem Ipsum has been the industry's standard dummy text ever since the 1500s, when an unknown printer took...
View Profile