Implementing AI/ML at Every Phase of Clinical Trials
Clinion seamlessly incorporates AI/ML into various facets of the clinical trial process, improving efficiency, accuracy, and insights throughout the trial lifecycle.
AI-Enabled CDASH Coding
- Clinion has implemented an AI enabled CDASH coding tool which automatically annotates custom form annotations with CDASH annotations.
- Once an eCRF form design is completed, users can choose to convert all the pages into CDASH annotations. Simply click on AI CDASH annotation and the AI tool will automatically annotate each field value to CDASH with CDASH label, annotation and domain.
- Users can review and accept the annotation or can edit for manual annotations or custom annotations.
- CDASH annotated CRF and SDTM reports can be generated without data transposition and external experts, saving time and money.
eProtocol Generation
- Clinion uses advanced GenAI tools to generate the complete study protocol from just the protocol synopsis.
- Clinion’s eProtocol generation tool has been trained on hundreds of real world protocols.
- Clinion utilizes the standardized Trancelerate protocol template. Simply upload the protocol synopsis and the tool generates each section of the protocol individually.
- Users can then collaborate and edit and refine each section of the generated protocol.
Effortless Remote Source Data Validation
- Streamline your source data validation process with Clinion’s AI-enabled Remote Source Data Review feature.
- The system intelligently extracts data from source documents and automatically cross-references with EDC data.
- Any discrepancies prompt the generation of queries, which get automatically assigned to sites.
- Say goodbye to time consuming and costly on site monitoring as well as manual document review and validation.
Smart GenAI Query
- Manual Data Review using AI and Automation!
- Data Managers need no longer go page by page or depend upon Biostatisticians to provide data sets to review and raise queries.
- In a first of its kind tool, Clinion has developed the GenAI-powered Prompt Bar where Data Managers can use simple English to create complex data sets on the fly!
- Review the data and raise queries from the report itself instead of going back to the CRF.
- Accelerate your trials by improving data quality and productivity!
Intelligent Chatbot Support
- Our intelligent chatbot uses Conversational AI to provide users with a knowledge repository, equipped with insights from hundreds of studies.
- Access user manuals, study information, and more with a simple free-flowing chat interaction, reducing site, CRO and Sponsor queries and tickets, streamlining operations and improving productivity.
AI Medical Coding for MedDRA & WHODD
- AI-driven medical coding is at the core of Clinion’s Machine Learning capabilities.
- By leveraging ML algorithms, our Medical Coding tool simplifies labeling tasks and facilitates rapid search functionalities to provide coders with the top matches, streamlining the coding process with enhanced accuracy and speed.
- Clinion’s AI medical coding supports both MedDRA and WHODD dictionaries, allowing coders to automate both Adverse Events and Conmed coding.
GenAI Charts On The Fly
- Create custom data sets across sites, subjects, visits, pages and fields by simple selection and without the requirement of complex statistical tools!
- These reports can be saved, scheduled, emailed or linked to third party tools via API.
- Create custom charts on the fly using Clinion’s GenAI chart generator from these data sets.
- Charts can be a bar, pie, stack, box, scatter and many more. Share these charts with others!
CSR Documentation Simplified
- Leverage our Automation & AI/ML capabilities to automate 60-70% of your Clinical Study Reports (CSR).
- Clinion Document Automation solutions use inputs of Protocol, SAP (Statistical Analysis Plan) and TLFs (Tables, Listings & Figures) to populate a standardized or custom CSR template and generate the CSR in MS Word format.
- CSR Automation supports collaboration and review across teams reducing first draft timelines significantly.
Experience the power of AI/ML in clinical trials Accelerate trials and reduce costs using AI!
