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.
• Nearly two decades of working experience in the Pharmaceutical Industry. • Currently working as Vice President & Head of Quality at Centaur Pharmaceuticals Pvt. Ltd. • Worked as Head...
View Profile
Pharma Techops, Quality, Regulatory professional, 25+ yrs experience in QA, QC, Analytical Development, QMS Integration, Regulatory, APIs and Formulations. Successful regulatory audits USFDA, EUGMP, WHO, TGA, Cofepris. Handled several USDMFs,...
View Profile