CSR Automation
AI That Writes Your CSR
Faster, Smarter, and Regulatory-Ready.
Writing a Clinical Study Report is Complex & Time-Consuming - Clinion AI Changes That.
Traditional CSR writing requires weeks of manual effort, extracting information from protocols, SAPs, TLFs, and raw datasets. Clinion AI automates CSR generation, intelligently assembling structured content to accelerate timelines, reduce costs, and ensure submission-ready accuracy.
AI extracts key study insights and auto-populates structured CSR sections. Your team reviews and finalizes them.
Seamlessly integrates Protocol, SAP, and TLFs to ensure every CSR aligns with ICH E3 guidelines and global regulatory standards.
AI auto-structures complex datasets into clear, well-formatted reports. No more copy-pasting from multiple sources.
Reduce CSR Timelines
Seamless EDC Integration
No new tools or complex training needed. AI coding happens within Clinion EDC in real-time.
Upload Study Documents
AI scans Protocol, SAP, and TLFs to extract relevant content.
AI Populates CSR Sections
Automatically fills structured sections, ensuring consistency and compliance.
Human Review & Refinement
Medical writers review AI-generated content and refines any insights provided.
Submission-Ready CSR
Finalized CSR is fully formatted and structured, ready for regulatory submission.
Why Clinion AI is the Trusted Choice for Clinical Trials
Purpose Built, Not Generic
AI models tailored for accuracy and precision in clinical research.
Audit-Ready & Compliant
Every AI output is logged, traceable, and meets global regulations (ICH, FDA).
Responsible AI, In Control
Clinion ensures transparency, accountability, and human oversight at every step.
AI Governance & Compliance
ISO 42001-certified for secure, ethical, and regulatory-aligned AI deployment.
AI That Lets You Generate CSRs Faster,
Without the Manual Burden.
Discover how Clinion AI transforms CSR writing – ensuring faster,
more accurate, and submission-ready reports