Webinar - The new QMS Normal Post COVID19 for the Pharma, Life Sciences & Medical Device Companies


Personnel Involved

Pharmacovigilance Auditor and Quality Consultant

  • Over 13 years’ experience working in pre- and post-marketing Pharmacovigilance (PV) and GCP, both as an auditor and in operational roles. Performed the role of Lead Auditor in a wide range of external and internal GVP audits and GCP audits in multiple Global territories.

  • Active support of regulatory inspections including US FDA, MHRA and Health Canada inspections as an Inspection Coordinator

  • Diversified experience in conducting CSV audits, ISMS audits, Process excellence, Training and Coaching

  • Conducted Audits globally across multiple territories including Europe, Americas, Asia, Middle East

  • Comprehensive knowledge and experience in the application of PV regulations, PV inspection readiness and training

  • Comprehensive knowledge and experience in the application of GCP, GMP, inspection readiness and training

  • For System Demo and further information, please call +91 98100 68241 or mail us at bd@crqa.in