Simplify Medical Document Processing and Submission

Healthcare and life sciences (HLS) organizations face challenges with inefficient document workflows that lead to operational ineffectiveness, errors, and compliance problems

To address these issues WinWire built an intelligent clinical document automation solution that can greatly enhance the quality of medical documentation to meet regulatory standards and guidelines.

Clinical Document Automation

WinCDA – WinWire Clinical Document Automation

Streamline Protocol and Clinical Study Reports with AI-Driven Automation

WinWire Clinical Document Automation Solution leverages Generative AI and natural language generation (NLG) to revolutionize drug development. By streamlining the creation and review of clinical trial documents, our platform speeds up time-to-market for new drugs and significantly reduces the risk of human error.

The solution generates documents such as informed consent forms and clinical study reports that comply with regulatory standards set by the FDA, EMA, and ICH, ensuring that users meet regulatory requirements.

Solution Features

Medical Document Automation
Enhanced Accuracy and Compliance Assurance

Detects errors, inconsistencies, and deviations from regulatory standards that human reviewers mistakenly overlook.

Healthcare Document Automation
Faster Review Cycles and Time Savings

Document review times are significantly reduced. This improved efficiency leads to shorter lead times for launching clinical trials and bringing new drugs to market.

Clinical Study Report
Improved Risk Mitigation and Patient Safety

Identifies potential safety concerns or ethical issues within clinical trial protocols. It can cross-reference historical data, adverse event reports and best practices.

AI Document Automation
Faster Approvals

Minimize review cycles with automation that generates formatted documents, reducing errors and the need for extensive edits.

Clinical Document Automation

WinCDA – Results You Can Expect

Consider our GenAI powered solution to boost efficiency, cut costs, and accelerate time-market for new drug development.

  • Clinical Study Report (CSR) – Reduces the time required for CSR report writing, allowing for faster and more efficient documentation processes.
  • Clinical Trial Narrative – Effortlessly generate tables and narratives for patient safety, enhancing accuracy and efficiency in reporting.
  • Protocol Summarization – Achieve comprehensive and precise summaries effortlessly, saving time and ensuring consistency.
  • Summary Clinical Safety – Automate the creation of module summaries, ensuring consistent and precise safety data reporting.

Optimize Your Clinical Trial Process – From protocol creation to CSR submission

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