Turnkey generation of submission-ready SEND datasets. Accelerated by Xbiom™ AI for 100% consistency and zero rejection guarantee.
Our proprietary AI-assisted technology reads and extracts data from LIMS, PDF study reports, and legacy documents with unprecedented accuracy.
Converts PDF tables and text into structured data, handling complex layouts and scanned pages.
Digital Study Report (DSR) generation ensures perfect alignment between source documents and SEND domains.
Accurately regenerates Trial Design domains from protocol text and summary tables.
Precision engineering meets regulatory expertise.
Datasets meet strict Technical Rejection Criteria (TRC) for FDA & PMDA.
Industry-leading delivery times with expedited options for urgent submissions.
Automated workflows significantly reduce manual effort and associated costs.
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