
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.
Total 25+ years of Experience in the AR&D, Expertise in end-to-end analytical project management on API NPD which include AMD, Std Management, Impurity qualification, AMV, AMT, CV and STP. Assist...
View Profile• 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 ProfilePharma 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,...
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