Biostatistics
Strategic planning, data analysis, and responses to regulatory review queries, ensuring robust and scientifically sound statistical methodologies.
Contract Research Organization
Guiding your clinical trials to success
AvanSight combines decades of clinical research expertise with AI-driven insights and proprietary IT solutions to accelerate innovation, optimize trial design, and maximize clinical success rates.
- 3xFaster delivery through software automation
- 30+Years of combined pharma and FDA experience
- 2020Serving sponsors of every size since
- AllTrial phases supported end to end
Our mission
Accelerate the development and approval of new drugs and devices through innovative approaches and advanced technologies.
Our services
Support across the full trial lifecycle
From protocol design through regulatory submission, each service is delivered by senior reviewers and backed by our own trial decision-support platform.
Statistical Programming
A cutting-edge platform that supports sophisticated trial design and comprehensive reporting across the full spectrum of your statistical needs.
Clinical Data Management
Support for protocol design, data capture, thorough analysis, and reporting for all phases of your trial.
Medical Writing Consulting
Expert medical writing consultation to maximize your chances of regulatory approval.
Compliance Review
A complete suite of pharmacovigilance services, ensuring full compliance and maintaining the highest standards of quality and safety.
Data Quality Review
Meticulous review of your data to guarantee its integrity and quality, preventing unnecessary delays in regulatory submissions.
How we work
A partnership, not a transaction
We stay involved from the first design decision to the final review query, so nothing is handed off and rediscovered later.
- 01
Trial design consultation
We work through protocol and endpoint decisions with medical reviewers and statisticians before the first patient is enrolled.
- 02
Statistical data review
Automated and human quality control run at every step, so issues surface while there is still time to act on them.
- 03
Regulatory submission support
Reporting, medical writing, and responses to review queries, prepared for the standards your submission will be held to.
A modern CRO
Cutting-edge technology, senior expertise
We offer expert advisory and trial management support while ensuring rapid project turnaround and flawless data integrity.
Technology-driven
- Modern software automation speeds up delivery by 3 times.
- Automated and human quality control at every step.
- Internal platform with zero setup required.
Led by experts
- Led by medical reviewers and statisticians with over 30 years in pharma and the FDA.
- A vast network of expert support for all drug studies.
Ready to talk through your trial?
Tell us where your study stands today and we will show you what our team and platform can take off your plate.