CLIN STREET mNote
mNote
Simplify monitoring visit scheduling and data collection with mNote, your all-in-one solution.
ISO 27001
HIPAA
21CFR Part 11Simplify Your Monitoring Workflow
Schedule Monitoring Visits
Easily plan, schedule, and manage all clinical trial monitoring visits from a single platform.
Gather Real-Time Data
Collect and track real-time monitoring visit details to ensure accurate site performance tracking.
Generate Monitoring Reports
Instantly create formal monitoring visit reports, confirmation letters, and follow-up letters, all within one centralized solution.
Why Choose mNote?
Visit Analytics
- Get instant insights on Visits and Report Submission
- Monitor site progress with detailed visit tracking metrics
- Easily check which reports are submitted or pending
- Identify submission delays and address them quickly
- Track and manage follow-up items
Built-in Templates
- Create confirmation and follow-up letters in seconds
- Customize built-in templates to fit your study needs
- Ensure consistent formatting in all communications
- Keep letters compliant with regulatory standards
- Automate letter creation to save time
Data Gathering and Reports
- Collect detailed monitoring visit data on-site
- Generate follow-up tasks from collected data
- Utilize built-in templates for quick and compliant reports
- Ensure 21 CFR Part 11 compliance for all documentation
- Experience an interface that simplifies data collection
Findings and Follow-ups
- Actionable Insights
- Proactive Solutions
- Issue Management
- Efficient Tracking
- Continuous Improvement
Discover How Our Platform Can Simplify Your Clinical Trials