No seat minimums. No surprise charges. Plans built for startups validating a batch and enterprises processing thousands of records per year.
For early-stage pharma and biotech teams validating batch record workflows.
For established QC departments running multiple product lines.
For regulated manufacturers with high-volume, multi-site operations.
All plans include electronic signatures, complete audit trails, version-controlled product specs, and validated export formats accepted by FDA inspectors.
Run a live trial with your actual batch records. No sales call required to start.