FOR SPONSORS & CROs
A Reliable Clinical Research Partner
AuraFi delivers high-quality data, operational excellence, and exceptional communication to help your study succeed on time and on target.
Quality & Technology
AuraFi leverages advanced technology and rigorous quality systems
to deliver accurate data, ensure compliance, and protect your study.
eSource Workflows
Real-time data capture and source verification to improve accuracy and reduce query cycles.
Electronic Regulatory Documentation
eTMF and eReg solutions for complete, traceable, and inspection-ready records.
Secure Data Handling
Enterprise-grade security, validated systems, and role-based access to protect data integrity and privacy.
SOP-Driven Quality Control
Standardized SOPs, QA oversight, and continuous monitoring to ensure consistent, high-quality execution.
Study Start-Up Process
A streamlined, proven approach to get your study up and running—
efficiently, compliantly, and on schedule.
01
Feasibility
Assess protocol, patient population, and site capacity.
02
CDA/NDA
Execute confidentiality agreements and study documents.
03
Site Qualification
Complete pre-qualification and confirm site readiness.
04
Regulatory Submission
Prepare and submit documents for IRB and regulatory approval.
05
Activation
Finalize training, systems, and logistics to go live.
06
Recruitment
Implement recruitment strategies and enroll qualified participants.
START YOUR STUDY
Request Feasibility
Tell us about your study and we’ll provide a complimentary feasibility assessment tailored to your goals.
Targeted Insights
Understand enrollment potential and site suitability in your therapeutic area.
Data-Driven Guidance
Receive expert feedback and real-world data to inform your study planning.
Trusted Partnership
Work with a dedicated team committed to your study’s success.