
Grade CTCAE Adverse Events with 95% Accuracy in Under 90 Seconds
CTCAE AI Agent helps oncology teams improve clinical trial documentation accuracy and patient safety monitoring
4.95 Based on 200+ reviews

Accuracy matching oncologist consensus
Processing time per adverse event
Annual revenue recovery per hospital
Manual CTCAE Grading vs. CTCAE AI Agent
See how CTCAE AI Agent transforms 15 minutes of manual work into 90 seconds of automated precision
9:30 AM - The Documentation Burden
Mrs. Chen reports nausea and fatigue from her chemo. You need to grade these adverse events per CTCAE v6.0. Was the nausea Grade 2 or 3? You flip through the reference guide while she waits. 10 minutes later, you're still documenting instead of treating. You're running 20 minutes behind.
12:15 PM - The Missed Safety Signal
Mr. Johnson mentioned "tingling in hands" last week. His labs show dropping platelets. These could be dose-limiting toxicities, but you're juggling 50 trial patients. The connection slips through. Safety event unreported. Compliance risk.
3:30 PM - The Inconsistent Grading
Your partner graded similar nausea as Grade 2 yesterday. You marked it Grade 3 today. The CRO monitor flags the inconsistency during the next audit. More time explaining variations instead of patient care. Trial data integrity questioned.
7:00 PM - The Revenue Leak
You're still catching up on documentation from today's 14 patients. Incomplete AE reports mean delayed billing. The hospital's revenue cycle team flags another $47,000 in denied claims tied to adverse event documentation gaps.Burned out. Revenue lost. Compliance risk growing.
Data-Backed Outcomes for Oncology Teams
See how AI-powered CTCAE grading improves accuracy, accelerates documentation, and protects oncology revenue — validated by real-world clinical use.
Experience CTCAE AI Agent in Action
Watch CTCAE AI Agent analyze complex cases, attribute symptoms to drugs, and grade adverse events with expert-level reasoning—in under 90 seconds.
Clinical Note
AI Analysis Process
Patient Context Extraction
Analyzing demographics, diagnosis, and treatment history
Symptom Pattern Recognition
Identifying clinical symptoms and severity indicators
CTCAE Criteria Mapping
Applying CTCAE v6.0 grading standards to findings
Drug Attribution Analysis
Determining drug-specific toxicity relationships
Evidence-Based Grading
Assigning grades with clinical reasoning
Confidence Assessment
Evaluating analysis reliability and evidence quality
Why Oncology Teams Choose CTCAE AI Agent
Three measurable improvements across clinical trials, cancer centers, and community practices
Improve Grading Accuracy by 43%
Achieve 95.8% inter-rater agreement vs. 67% manual baseline. Reduce protocol deviations and improve patient safety.
Ensure consistent CTCAE grading across trial sites
95.8% accuracy
Reduce Documentation Time by 90%
Grade adverse events in under 90 seconds instead of 10-15 minutes. Oncologists save 5+ hours per day.
Spend more time with patients, less on paperwork
5+ hours saved daily
Recover $1.2M-$2.5M Annually
Increase adverse event charge capture from 60% to 95%. Accurate drug attribution improves reimbursement rates.
Protect revenue with compliant, billable documentation
$1.2M-$2.5M recovered
Join Leading Oncologists Already Using CTCAE AI Agent
From academic medical centers to community practices, oncology teams trust CTCAE AI Agent for accurate, compliant adverse event grading.
Built for HIPAA Compliance from Day One
CTCAE AI Agent meets the highest healthcare security standards, protecting patient data while delivering clinical-grade insights. Our platform is designed with healthcare-specific regulations and enterprise security at its core.
Data encrypted in transit and at rest
Frequently Asked Questions
Ready to Transform CTCAE Grading with CTCAE AI Agent?
Join oncology teams already using CTCAE AI Agent to improve patient safety, accelerate documentation, and recover lost revenue.
HIPAA Compliant
EHR Integration Ready
30-60 Day Setup
SOC 2 Type II Certified





