Support, privacy and release notes
- v1.3 — SAS codegen + reverse spec drafting: base SAS backend (no special licenses) and Path B: draft a metacore-style ADaM spec straight from your annotated mocks.
- v1.4 — define.xml 2.0 generation: export define drafts from Path B and re-upload them for round-trip verification; templates stay aligned to the cardinal (FDA safety tables) catalog with an automated drift check.
- v1.5 — Data Readiness Report, tfrmt JSON interop, Dataset-JSON v1.1 input, PPTX review decks: drop CSV headers or Dataset-JSON files to see which TLFs can run right now.
- v1.6 — Validation Evidence Pack (starter) + mockgen-mcp: a CSA-style IQ/OQ scaffold generated from your project's actual evidence, plus a five-tool MCP server for Claude Code, Copilot and Cursor.
- Supported imports: project JSON; DOCX with Heading 3 titles such as Table 14.1.1 Demographics followed by a table; define.xml 2.0; specification XLSX sheets Datasets, Variables, ValueLevel, Codelists and Methods; tfrmt display-layer JSON subset. Complex Word layouts and tfrmt body_plan are not restored. Use project JSON for full project recovery.
- Generated programs and reports: SAS, base R and pharmaverse code are scaffolds, not executed results. Readiness checks column availability, not data quality. DOCX, PDF and PPTX outputs need independent layout and content review.
- Project import limits: 10 MB JSON, 1,000 modules, 10,000 rows per module. Keep projects smaller for responsive editing.
- Core processing stays in your browser — runtime libraries are served with this tool, with no external CDN required. A fresh page still needs access to this website or a local server. Projects and settings use browser storage. Optional experimental AI sends prompt content to your selected provider and may incur provider charges.
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