CliniWiseAI
Transforming Clinical Trials Through AI, Machine Learning, and Generative AI
Integrating AI and ML Throughout All Stages of Clinical Trials
Embrace the future of clinical research with innovative AI solutions tailored for the clinical trial process. CiniWiseAI seamlessly weaves AI and ML into various aspects of the clinical trial process, enhancing efficiency, accuracy, and insights across the entire trial lifecycle.
The Building Blocks
CliniWiseAI offers a suite of innovative solution components that empower researchers to achieve better outcomes and drive innovation in clinical trials.
eProtocol Creation
eCRF & eCSR Generation
Patient Narrative & Case Narrative
Automated Data Extraction
PHI Redaction
eSDV Assistant
Chat with Citation
CliniWiseAI leverages advanced GenAI to create a complete study protocol from just the protocol synopsis. Our eProtocol generation tool is trained on hundreds of real-world protocols, ensuring high-quality outputs.
Simply upload the protocol synopsis, and the CliniWiseAI will generate each section of the protocol individually like objectives, inclusion and exclusion criteria etc. Multiple Authors / Users can then collaborate, edit, and refine each section of the generated protocol as needed and prepares first draft within days.
eProtocol Creation
CliniWiseAI is revolutionising the way Case report forms ( CRFs) & Clinical Study Reports (CSRs) are created with cutting-edge AI/ML automation. By automating up to 70% of the process, our solution takes inputs like Protocol, SAP, and TLFs to effortlessly generate a CSR draft and eCRFs in MS Word format.
This helps in faster collaboration, quicker reviews, and a dramatic reduction in the time it takes to get from raw data to a polished report. Say goodbye to manual drafting and hello to smarter, more efficient clinical reporting
eCRF & eCSR Generation
CliniWiseAI redefine the creation of Patient and Case Narratives in medical coding. By integrating advanced AI/ML, our solution simplifies the extraction of key clinical information from patient records, generating detailed narratives that are both accurate and consistent.
This not only enhances coding precision but also accelerates the process, reducing manual errors and saving valuable time. Get high-quality narratives that support your coding needs faster and with greater confidence.
Patient Narration & Case Narration
CliniWiseAI advanced OCR-driven solution automates the extraction of critical data from drug safety documents, transforming them into structured text with remarkable accuracy.
By seamlessly converting scanned documents into actionable data, our platform automatically fills EDC (Electronic Data Capture) systems, eliminating manual data entry. This not only speeds up the process but also reduces errors, ensuring that your drug safety data is consistently accurate and ready for analysis—faster than ever before.
Automated Data Extraction
CliniwiseAI PHI Data Redaction solution ensures that patient privacy is always maintained by automatically removing personal health information (PHI) from DICOM and JOG files.
Using advanced algorithms, our platform scans and redacts sensitive data, such as patient names and IDs, while preserving the integrity of the medical images. This streamlined process helps you comply with privacy regulations, minimize risk, and protect patient confidentiality without compromising data quality.
PHI Redaction
eSDV Assistant
CliniwiseAI enhances your source data validation process by intelligently extracting data from source documents like Drug safety documents, lab reports and automatically cross-referencing it with EDC data.
When discrepancies arise, queries are generated automatically and assigned to the respective sites.
Say goodbye to time-consuming and costly onsite monitoring, as well as manual document review and validation.
CliniWiseAI our intelligent chatbot employs Conversational AI to offer users a comprehensive knowledge repository, enriched with insights from hundreds of studies.
With a simple and fluid chat interaction, you can access user manuals, study information, and more, significantly reducing queries and tickets from sites, CROs, and sponsors. This streamlines operations and boosts productivity while enhancing the overall user experience.
