Meta-Xceed, Inc. (MXI) builds software and delivers services for pharmaceutical, biotech, CRO, and medical-device teams — from CDISC data transformation to regulatory submission. Our flagship product, DoLoup, brings agentic AI automation to clinical statistical programming.
Trusted standards, regulated environments
DoLoup writes the SAS program, runs it, reads the real log, fixes the ERRORs — and loops until it's clean. Then it QCs every dataset against your CDISC checklist with an independent validation program written by a different AI model.
A senior team supporting clinical programs across the full regulatory lifecycle.
SDTM and ADaM conversion, define.xml data definition, and submission-ready deliverables aligned to your IG version.
SAS 9.4 and R programming for tables, listings, and figures — accelerated by DoLoup's agentic automation.
Analysis planning, statistical review, and support for electronic submissions to regulatory agencies.
SAS server installation on-premise or cloud, IQ/OQ/PQ validation documentation, and tooling like Pinnacle 21 and R.
CRF design, database builds, discrepancy management, and delivery in CDISC models.
Purpose-built clinical software with 21 CFR Part 11 compliance and full validation documentation.
Clinical data expertise built study by study since 1997.
Talk to us about DoLoup, or about supporting your next study from raw data to submission.
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