Accelerate scientific discovery and maintain rigorous compliance. We engineer scientific data management systems (SDMS), biobank specimen inventory, and clinical trial sample tracking platforms adhering to 21 CFR Part 11 and GLP standards.
Comprehensive digital infrastructure for biobanks, molecular pathology labs, and clinical trial sponsors.
Hierarchical visual freezer mapping (-80°C to LN2 cryovessels), 2D barcode aliquot tracking, freeze-thaw cycle monitoring, and chain of custody logging.
Immutable audit trails, dual-factor cryptographic signatures, and audit-ready data versioning satisfying FDA GxP requirements.
Protocol definition engines, assay run orchestration, plate layout design (96/384-well), and automated dilution calculations.
Automated bi-directional data capture from mass spectrometers, HPLC systems, PCR analyzers, and sequencers via RS-232 and REST APIs.
Multi-site visit schedule mapping, subject de-identification, kit requisition dispatch, and blinded protocol compliance.
Automated Levey-Jennings charts, Westgard rules evaluation, calibration curve fitting, and batch validation workflows.
Speak with our laboratory informatics and compliance engineering team.