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Accelerate Your Clinical Research Documentation with AI

Generate comprehensive protocols and informed consent forms in minutes, not days, with our AI-powered platform.

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Study Protocol
ICF
Statistical Analysis Plans
Investigator Brochures
Clinical Study Reports
Patient-Facing Materials

Tired of Spending Weeks Drafting Clinical Documents?

Creating protocols and informed consent forms is a critical but time-consuming process. Researchers face multiple challenges that our AI solution solves:

Time Efficiency
Reduce drafting time from weeks to hours for protocols and ICFs
Regulatory Alignment
Built-in compliance with ICH-GCP and regional requirements
Quality Assurance
Consistent structure and comprehensive coverage of required elements
Collaborative Workflow
Streamlined review process and version control for your entire team

How It Works

Our AI-powered platform simplifies clinical documentation while maintaining the highest standards of ethics and regulatory compliance.

01

Select & Input

Choose your document type (Protocol or ICF) and enter key study details through our guided workflow.

02

AI Generation

Our advanced AI creates a comprehensive first draft with all required sections, tailored to your specific study needs.

03

Review & Finalize

Review, customize, and export your document in multiple formats to share with your team or IRB.

Comprehensive Document Support

Our platform provides specialized AI-powered generation for both study protocols and ICFs.

Study Protocols
  • Comprehensive protocol structure with all ICH-GCP required sections
  • Customizable sections for study design, endpoints, and eligibility criteria
  • Adaptive templates based on study phase and therapeutic area
  • Consistency checks across all protocol sections
  • Integrated references and glossary management
Informed Consent Forms
  • All required ICF elements per regulatory guidelines
  • Plain language optimization with readability scoring
  • Automatic risk and procedure extraction from protocols
  • Country and population-specific adaptations
  • Visual element integration for enhanced comprehension
"This platform has transformed our documentation process. What used to take weeks now takes hours, with better quality and consistency. The AI-generated protocols and ICFs have accelerated our study start-up time by 40%."

Dr. Sarah Johnson

Principal Investigator, Clinical Research Institute

Built by Researchers

Created by clinical research professionals who understand your documentation challenges

Regulatory Excellence

Adheres to ICH-GCP, FDA, EMA, and international regulatory requirements

Enterprise Security

SOC 2 compliant with end-to-end encryption to protect your sensitive study information

Accelerate Your Clinical Research Documentation Today

Join research teams worldwide who are saving weeks of documentation time while improving quality and compliance.

Start 14-Day Free TrialSchedule a Demo

No credit card required. Cancel anytime.

Expanding to Meet Your Documentation Needs

We're constantly evolving our platform to support more clinical research document types. Coming soon:

Statistical Analysis Plans
Investigator Brochures
Clinical Study Reports
Patient-Facing Materials
Regulatory Submissions