FDA Compliance and Clinical Trial Computer System Validation 2019

  • 27 Feb 2019
  • Webinar

Description

Topics
  • Computer System Validation (CSV) Methodology
  • FDA GxPs
  • Risk Management
  • System Development Life Cycle (SDLC) Framework
  • Compliance Strategy
  • GAMP 5
  • Industry Best Practices
  • Cost vs. Compliance
  • Training
  • Policies and Procedures
  • Leveraging Vendors
Who should Attend
  • Data Stewards
  • Data Owners
  • Information Technology Developers and Testers
  • Information Technology Analysts
  • Clinical Data Managers and Scientists
  • QC/QA Managers and Analysts
  • Compliance and Audit Managers
  • Analytical Chemists
  • Automation Analysts
  • Laboratory Managers
  • GMP Training Specialists
  • Computer System Validation Specialists
  • Business System/Application Testers
  • Business Stakeholders/Subject Matter Experts

Past Events

Important

Please, check "FDA Compliance and Clinical Trial Computer System Validation" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Management, Quality assurance
Technology: Data management, Information Technology (IT)

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