Say goodbye to paper casebooks. From eCRF authoring to AI analysis, the entire clinical data journey on a single screen.
From study design to data lock. Replace paper casebooks with eCRF, manual work with AI.
Build protocol-specific electronic case report forms online and save them instantly. Organize data by visit, and everything you type is automatically saved.
From enrollment to follow-up at a glance. See who is being screened, who has been randomized, and track dropout/completion status in real time.
Manage multi-site studies in one place. Set granular access permissions per site and investigator, and track protocol versions.
Manage PI and CRC roles and permissions separately. Build teams per site and log who performed which task.
Get immediate alerts on anomalous inputs. When data errors are found, issue queries and track resolution. GCP-compliant.
Export collected data to Excel or PDF. Build statistical analysis datasets and generate monitoring reports instantly.
Hover over 50+ medical terms including CDISC standard terminology, medical abbreviations, and lab indicators to see definitions. Administrators can add and edit institution-specific terms.
Automate clinical data analysis, error validation, and report writing with cutting-edge AI technology.
AI automatically analyzes subject eCRF data. Provides clinical interpretation and outlier detection for physicians, and easy-to-understand summaries with lifestyle tips for subjects.
Click the AI button at the bottom right to start a conversation. On subject screens, the AI uses that subject's data for more accurate answers.
When saving case records, AI automatically detects medically implausible values. "BP 200/300?" "Age doesn't match diagnosis?" — errors flagged instantly.
AI automatically finds and evaluates adverse events in eCRF data. Analyzes severity (mild to serious) and causality, and provides instant alerts with reporting checklists for serious AEs.
Upload a clinical protocol and AI auto-generates a CRF draft. Say "add a blood pressure measurement" in natural language, and AI edits the CRF with CDASH/SDTM standard mapping and quality review.
AI drafts monitoring reports based on eCRF data after CRC visits. Auto-detects protocol violations and exports to multi-sheet Excel format.
Bring Project progress, Site activity, capacity, and Query trends together in one evidence-linked view.
"Will my subject data leak?" — the biggest concern in clinical settings. eCRF complies with international web standards and OWASP security practices, with data protection designed from the ground up.
When requesting AI data analysis, subject names, birth dates, and registration numbers are automatically removed server-side. AI never knows whose data it is — only anonymized analysis results are returned for clinical use.
The information you can view differs depending on your assigned role — PI, CRC, monitor, etc. Even within the same project, you can only access your own subjects and site data.
CRF design documents are stored using the ARIA-256-GCM encryption algorithm — the same standard used by Korean government agencies for e-Government security. Unauthorized access is absolutely impossible.
Security headers, content policy, cross-origin restrictions, code injection prevention, and brute-force password defense — a 5-tier protection system detects and automatically blocks external attacks. Compliant with W3C web standards and OWASP international security practices.
Real-time firewall automatically detects and blocks abnormal access attempts. Admin access to servers is restricted to authorized IPs only, and an immediate response system activates when signs of external attack are detected. Regular security updates and vulnerability monitoring keep servers in optimal security condition.
Connect storage, backup, and recovery in a resilient framework that keeps clinical research moving.
Changes to subject data can be reviewed by the responsible administrator.
Simply signing up does not grant access to subject information. You must receive approval from the principal investigator to view study data. After 30 minutes of inactivity, you are automatically logged out for protection.
Do not leave every clinical CRF change to a development queue. Study teams can edit directly like Google Docs and structure visits, sections, and fields with drag and drop.
Project creation, site/PI/CRC assignment, access permission setup
Screening, randomization, and visit scheduling
Complete and save case report forms at each visit
Outlier detection, data analysis, and quality verification
Export to Excel/PDF and generate reports