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
Computer System Validation (CSV)
Process Validation
Equipment Qualification
Cleanroom Validation
Method Validation
