After decades working in labs and clinical trials, we kept seeing the same frustrating pattern: study samples getting mishandled, delayed, or lost—not because the science was flawed, but because the systems behind the scenes were broken. Sites relied on paper logs and spreadsheets. Labs received mislabeled or untracked samples. Sponsors had to reconcile messy data months later, costing millions in delays. Meanwhile, the patients who gave their time and blood to these studies had no idea their contributions might never be usable.

We built OverSite to fix that. It’s a platform designed to bring transparency, real-time tracking, and enforced compliance into sample workflows—from the moment a tube is picked up at the site to when it’s processed at the lab. We made it intuitive, interoperable, and fast to set up, because the people at sites already have enough to manage. OverSite replaces guesswork with barcode scans, timestamps, and automated alerts—so sponsors, sites, and labs are always on the same page.

This isn’t just about convenience. It’s about restoring trust in clinical research. When we lose a sample, we lose data. When we delay a trial, we delay life-changing treatments. And when we rely on memory and manual workarounds, we leave too much room for error. OverSite is here to close that gap—for the industry, and for the patients counting on us to get it right.