GoVal Validation Lifecycle Management System (VLMS) for Life Science Industries

Capability to maintain 100% electronic records, e-signatures and fulfil CFR Part 11 &  Annex 11 regulatory compliances.

Efficient, User friendly and Scalable Solution

Always On, Audit Ready & Transparent

Digital Transformation for your Validation processes

Process Standardization, Monitor and Control

End-to-End Validation Process

Key features

  • Perform GxP Assessments for your Validation Projects, define GAMP category and identify Validation deliverables.
  • Define User Requirements (URS), Specifications, Functional and Design Specification. Create Risk assessment, create and execute test cases, Auto generated Traceability Matrix
  • Automated workflow with electronic signature. Periodic review, Vendor Assessment
  • Validation Summary Report (VSR), Inventory Report and other key data reports
paperless validation

Computer System Validation (CSV)

paperless

Process Validation

paperless

Equipment Qualification

paperless

Cleanroom Validation

paperless

Method Validation

paperless

QMS Framework

Ready To Get Started?

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