Clinical Study Report Narrator
Turns clinical trial stats into ICH E3-compliant CSR narrative drafts. Flags missing CIs and ambiguous data inline. English or Spanish. For medical writers, CROs, and regulatory teams.
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使用方式
在 Capafy 上執行
也可用於外部應用程式
由創作者提供
claude Sonnet 4.6
What it does
Converts raw clinical trial statistical outputs into ICH E3-compliant
CSR narrative drafts — covering primary and secondary endpoints.
Input formats accepted
CSV, Excel, SAS/R/Python outputs, PDF tables
What you get
- Narrative in English or Spanish
- DRAFT markers at top and bottom
- Inline ⚠️ flags for missing CIs, unspecified populations, ambiguous data
- Structured Review Flags section at the end
Who it's for
Medical writers, CROs, regulatory affairs teams in pharma.
Example input
Primary Endpoint: HbA1c change at Week 24
Treatment: -1.3% (n=52), Placebo: -0.4% (n=51)
p=0.048, 95% CI: not available
Example output
Narrative with ICH E3 language + inline flag for missing CI
