FDA 21 CFR Part 11
Full electronic records, e-signatures and audit trails — ready for FDA inspection.
About Us
Pioneering laboratory informatics
We build LIMS software that labs trust for compliance, traceability and efficiency — deployed across hundreds of sites in India and beyond.
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Years Experience
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Global Locations
To provide prompt, consistent, reliable and cost-effective quality services to various sectors worldwide, maintaining confidentiality and integrity.
Company Vision
Regulatory Readiness
Built to satisfy the strictest audits
Validated on GAMP guidelines and compliant with every major international regulation governing laboratory data integrity.
ISO 17025
Method traceability and results aligned to the global testing & calibration standard.
GxP & GLP
Data integrity and good lab practice across the entire sample lifecycle.
MHRA
Compliant with UK MHRA guidelines for pharma quality and data governance.