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


Personnel Involved

Lead Auditor & Quality Consultant at US

  • Over 2 decades of experience within the Life Sciences Healthcare Industry demonstrating capability and expertise with - IT, Quality, CSV and Project Management in consulting and full time positions.

  • Strong background with IT/Quality governance and quality system development deliverables, process improvements, change management.

  • Sound understanding of the regulated space including FDA’s 21 CFR Regulations, ISO 13485 (Med Device QSR) and ISO 19011 (Management Systems Auditing) compliance, audits, industry best practices (cGXP – GMP, GLP and GCP), software quality assurance (SQA) and computerized systems validation.

  • Experienced with validation strategy/delivery and IT governance pertaining to Cloud/SOA/ SaaS based systems.

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