Between “the instrument finished” and “the chemist signed” sit two to three hours a day per analyst: processing the export, checking QC against your limits, working out which samples a failed check invalidates, building the import, writing the review record. Caddie does that in minutes and hands the chemist a batch ready to sign.
We read the raw instrument export and your SOP. The agent applies your QC limits, follows bracketing to its consequences per analyte, lists the re-runs with reasons, builds the LIMS import file and drafts the review record. Peaks and matrix judgement stay with your chemists.
Food, environmental and pharma labs, CDMOs and CROs share the same afternoon of data work, but the methods, limits and paperwork differ. Each gets its own setup.
Multi-residue panels with hundreds of analytes, and every customer with their own limits. The agent applies the right specification to the right client and drafts the certificate.
EPA methods are the same in every state, so a method built once runs everywhere. Bracketing, blanks and recoveries are followed to their consequences, and the corrective-action record is drafted while the run is still fresh.
Out-of-specification results carry federal teeth. Whether you are a sponsor's QC group, a CDMO releasing batches against each client's specification, or a CRO reporting stability and bioanalytical studies in the sponsor's format, the agent assembles the Phase 1 investigation from the chromatography data and audit trail, in your own template, so QC reviews evidence instead of hunting for it.
Results from agents running inside client businesses. Client names withheld; the numbers are theirs and we can walk you through how each was measured.
Out-of-spec results used to mean days of pulling audit trails, prep records and instrument logs by hand. The agent assembles the Phase 1 packet from the run data with every piece of evidence cited, and QC reviews and signs.
Analysts in food and environmental labs spent most of their day processing exports, checking QC and keying results. The agent now does it as each run finishes: import file, re-run list and review record ready before the analyst sits down.
On an ICP-MS run of 320 samples, a continuing calibration check drifted to 87%. The agent invalidated the ten affected samples for lead only, released the other 310, and produced the import file and record. The old way: a chemist re-derives it.
Labs told us the same thing: changing the LIMS takes years and sometimes fails. Caddie reads export files and produces import files. Nothing touches the instrument PCs; nothing about your LIMS changes.
Formatted for your LIMS and your test codes, with qualifiers applied. Upload and go.
Which samples, which analytes, which QC failure. Per analyte, not whole-sample reflexes.
The batch story written for analyst, reviewer and QA to read and sign. Audit trail included.
One method, one redacted batch: the export, the run sequence, your SOP and the signed results. We re-close it and show you it matches your chemists, sample for sample.