Data Reporting

Virco facilitates clinical trial data transfers to the sponsor or CRO’s specifications with the infrastructure, processes and flexibility required for smooth hand-offs.

• High-quality, customized reports
  • Data  quality checked prior to release
  • Documentation and validation to industry standards or beyond
  • Real-time or batch reporting
  • All customer requirements in terms of transfer frequency, format and method of transfer is upfront described in project specific data transfer agreements (DTA).
• Secure and supportive infrastructure
  • Proactive approach during operational set-up
  • Data cleaned, assessed for quality and uploaded for transfer to clients
  • Secure data transfer:
    • Results delivered to e-rooms, SharePoint, MBOX or secure client portals in pre-specified formats (SAS, Excel, txt, etc.)
• Established methodology for computer system validation
  • Fully 21 CFR 11 compliant
  • Provides peace of mind for dossier
• Flexibility for clients
  • Responsive to customer queries and needs
  • Ad-hoc requests and  prompt follow up on data-related queries
  • Frequency of data delivery can  be increased/decreased
  • Results available to client 24 hours/day, 7 days a week
  • Desired formats accommodated
• Extensive Virco technical and scientific guidance for transfer, set-up and delivery

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