Labs validate a pipeline once, carefully. Then it keeps changing, and the paperwork falls behind what is actually running.
I started Aver to close that gap with engineering, not paperwork: fingerprint every dependency, benchmark against public reference materials, measure every change, and produce evidence an inspector can verify.
Two decisions came first. Aver never touches patient data. And Aver produces evidence, not verdicts; your laboratory and your accreditor decide.
If revalidation keeps slipping in your lab, I'd like to hear how you handle it today.