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

Personnel Involved

Senior PV Consultant & Auditor at US

  • Pharmacovigilance and Medical Writing professional with over a decade (10 years+) with knowledge of ICSRs, PADERs, aggregate reports, signal management, REMS, peer reviews, manuscripts, protocols, and CSRs. Board member and contributor to the American Medical Writing Association (AMWA) Northern California.

  • Project Manager with proven record of successfully bootstrapping and delivering diverse multi-national projects (Mainly US, EU). Proficient in the use of standard project management practices.

  • Business development professional adept in Solution development, Lead generation, having handled multimillion-dollar global projects.

  • Quality and compliance professional with a track record of 14 internal audits, 11 client audits and 2 regulatory audits.

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