Clinical Study Report (CSR) Authoring
Clinical Study Report (CSR) Authoring
Say goodbye to long hours, version chaos, and manual edits. ZYLiQ’s AI-powered platform helps you create submission-ready Clinical Study Reports (CSRs) in record time-without compromising on quality or compliance.
Get AI-generated CSR drafts in just hours, not weeks.
ICH E3, TransCelerate, Sponsor's Template and compliance with 21 CFR Part 11.
Automated data pulls eliminate manual errors.
Work together in real-time with Word interface.
Fits your templates, formats, and table, figure interpretation in simple english.
Add protocol, TLF, and SAP. We handle the rest
Transform sections, structured summaries, in-text tables and figures
Work as a team in a familiar editor-track changes, leave comments
Fully formatted, audit-ready, submission-compliant
Auto-transform tables into in-text format.
Turn tables and figures into high-quality interpretation.
Automatically shifts content to past tense-ideal for final reports like CSRs.
Track every change, source, and contributor-so you're always inspection-ready.
ZYLiQ doesn’t just speed up CSR writing-it transforms it.
Let’s show you what AI-powered medical writing really looks like.