An Intuitive Platform for Optimized Clinical Protocol Design
Clinical trial leaders make critical decisions based on spreadsheets, instincts, outdated tools, and dozens of meetings and conversations.
Faro’s technology streamlines this process so that teams can make faster, better-informed decisions about protocol design.
Protocol Design
Optimize Study Design with Data-Driven Insights
Faro’s Study Designer enables clinicians and scientists to optimize clinical study designs, significantly reducing cost, patient burden, and other key trial performance measures. With minimal training, teams can create and configure study-defined procedures and access real-world metrics that allow them to see the impact of design choices. The Study Designer enables teams to dynamically modify the Schedule of Activities based on real-time feedback to optimize study requirements.
Collaborate in Real Time
The Faro Study Designer empowers teams to collaborate confidently on clinical trial designs, guided in real-time by data-driven insights. Users can explore various iterations of trial designs and assess their performance metrics, gaining quantitative insights into the impact of their design changes. By enabling synchronous teamwork, your team can address challenges, rapidly iterate on design changes, and streamline processes to minimize time and costs.
Navigate Complexity with Ease
The Faro Study Designer quickly generates reusable plain-language content to promote standardization and efficiency within or across clinical programs.
AI Co-Author
Improve Efficiency Without Sacrificing Quality
Faro combines the power of large language models with the industry’s most comprehensive repository of structured public clinical trial data to generate high-quality clinical protocol documentation. Faro’s proprietary evolutionary protocol generation architecture overcomes many of the shortcomings of standard LLMs, including hallucination, bias, lack of clinical understanding and tone, and lack of transparency. User feedback ensures that the model continues to learn and improve with time to suit your team’s specific preferences and needs.
Design Protocols with the Latest in Generative AI
Faro’s AI “Co-Author” streamlines initial protocol design by automatically generating a recommended baseline schedule of activities and other protocol components in a fraction of the time it would take to build manually. Sections can also be quickly regenerated as the trial design changes, flexibly adapting to how your teams work.
Author Downstream Documents With Ease
Leverage your protocol design to quickly and easily generate downstream documents, such as informed consent and other critical forms, freeing your team to focus their time on what matters most. Faro is constantly adding new clinical documentation to the roster of generated content it supports – connect with us to learn how we can augment your specific processes.
Downstream System
Integration & Digital Data Flow
Unlock Study Information Potential
Faro Health helps optimize your protocol design to manage the entire clinical development workflow’s complexities effectively. A digitalized protocol built with the Faro Study Designer allows you to efficiently utilize all study design information across the clinical trial continuum.
Enable Downstream Automation with Versatile Content Elements
Faro supports the output of structured, versatile protocol design elements in document format by seamlessly populating standard clinical templates that enable downstream automation. Users can create and curate reusable content elements during protocol design that easily adapt to other key downstream documents.
Align with Industry Data Standards
Faro connects structured protocol elements to industry data standards. Study design components, including the Schedule of Activities, can be easily configured for use in downstream data collection systems.
Ready to see Faro in action?
Set up a call to learn more about transforming your clinical trial protocol design.