You give it a study protocol. It returns a first-draft statistical analysis package — a fact sheet, a Statistical Analysis Plan, a set of mock TLF shells, and an analysis specification — in minutes instead of weeks.

1. Read — the protocol is parsed section by section and the study facts (design, population, endpoints, statistical methods) are extracted and consolidated.
2. Plan — the tool decides which Tables, Listings and Figures the study needs, following standard reporting conventions, and specifies each display's analysis (dataset, method, population, statistics).
3. Standardize — every recognised analysis variable is matched to its canonical clinical-standard definition (label, structure, Core status, a standard derivation template) so the specification is consistent by construction and traceable to a published standard authority — not invented per study.
4. Author — a full SAP draft is written, and the shells + analysis specification are rendered as Word and Excel you can hand to a statistician.

The standardization step draws on a curated library of standard analysis concepts. The library ships only published-standard definitions; no client study, sponsor content, or proprietary data is included or exposed.

Every draft is a starting point and must be reviewed by a qualified statistician before any regulatory use.