Manual QC was the bottleneck. And the risk.
Saol Therapeutics builds clinical kits — physical assemblies of swabs, brushes, labels and packaging that ship to research and treatment sites. Each kit carries a unique configuration of patient and sample IDs that must match an authoritative kit-construction sheet before release. A single mislabel can compromise a study.
The pre-existing process was paper-driven: an operator visually compared scanned barcodes against a spreadsheet, line by line, kit by kit. Slow on a good day. Brittle on a bad one. And critically, the audit trail of who-verified-what-when lived in handwritten records — not what a regulator wants to see.