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

Personnel Involved

Senior Pharmacovigilance Consultant & Auditor

  • Conduct Audits & Inspection Preparedness

  • Pharmacovigilance Systems Development & Review

  • Working knowledge of EU GVP, FDA (US), TGA, EU, Health Canada and DCGI Guidelines

  • Proficiency with use of Medical Dictionary for Regulatory Activities (MedDRA), MS-Office (Word, Excel, PowerPoint),

  • Safety databases including Oracle Argus and ARISg

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