Study Feasibility Questionnaire Support & Resources

Ryght AI is a United States based clinical trials AI software company that works with leading pharmaceutical sponsors and contract research organizations (CROs) worldwide to accelerate clinical trial site selection and feasibility processes.

We help bring new therapies to patients more quickly by streamlining the connection between pharmaceutical sponsors and qualified clinical research sites. Our AI-powered platform enables sponsors to identify the best-fit sites for their studies and accelerates the feasibility assessment process from months to weeks.r
Pharmaceutical sponsors and CROs use our Feasibility Accelerator platform to efficiently identify and contact qualified research sites for their upcoming clinical trials. When you receive an email from us, it means:
- A clinical research sponsor is conducting a real clinical trial and has identified your site as potentially well-suited for their study
- You've been selected based on your site's capabilities, therapeutic expertise, and historical performance
- This is an opportunity to be considered for selection for an upcoming clinical study
Frequently Asked Questions
IS THE EMAIL I RECEIVED A LEGITIMATE FEASIBILITY REQUEST?
Yes, Ryght is an established technology service provider.
The email you received is from a legitimate pharmaceutical sponsor or CRO who is using our platform to conduct their feasibility assessment. We never send unsolicited emails - you were specifically selected because your site matches the requirements for a real clinical trial opportunity.
We do not ask for passwords, credit card information, or sensitive personal data. The questionnaire is strictly focused on your site’s clinical capabilities (e.g., patient volume, equipment, and staff experience).
WHY HAVEN'T I HEARD OF RYGHT AI BEFORE?
Ryght AI was founded in 2023 and has been growing rapidly since then. While we may be newer than some traditional clinical trial technology companies, we're backed by major industry players (Accenture, Microsoft, NVIDIA) and work with established CROs like Biorasi and QPS Holdings. Our platform is already used by leading pharmaceutical sponsors and trusted by major academic medical centers including USC, Mayo Clinic, and the Medical College of Wisconsin.
HOW DID YOU GET MY CONTACT INFORMATION?
Your site information comes from publicly available data sources, including clinical trial databases, institutional websites, and our network of 100,000+ clinical research sites. When sponsors use our platform, they select sites based on specific criteria such as therapeutic expertise, patient populations, and historical trial performance. Your site was identified as a strong potential match for their study requirements.
IS THERE ANY COST TO COMPLETE THE FEASIBILITY QUESTIONNAIRE?
No, absolutely not. Completing the feasibility questionnaire is completely free for research sites. Our platform is paid for by the pharmaceutical sponsors and CROs who are seeking qualified sites for their trials. Research sites can access and use our feasibility tools at no cost.
If you create an account with us, you can see
WHO SEES THE INFORMATION THAT I SUBMIT?
The information you provide in the questionnaire is delivered directly to the Clinical Operations or Study Team at the sponsoring company listed in your email. It is used to determine if the study is a good fit for your research site's capabilities.
WHAT HAPPENS TO MY DATA?
Data security is our top priority. Ryght AI is SOC 2 Type 2 compliant, which means we meet rigorous security standards used by Fortune 500 companies. Your feasibility responses are only shared with the specific sponsor or CRO who sent the request. We use enterprise-grade encryption, maintain HIPAA-aligned practices, and never sell or share your data with unauthorized parties.
WHAT IF I DON'T WANT TO BE CONSIDERED FOR THE STUDY?
That's completely fine. Completing the questionnaire doesn't commit you to anything. It firstly informs the sponsor whether or not you would like to be considered, and secondly if your site is a good fit. You can decline to participate by responding "no" to the question "Are you interested in participating in this study?"
If you'd prefer not to receive future feasibility requests, please let us know through the contact form below.
WHAT HAPPENS AFTER I SUBMIT THE QUESTIONNAIRE?
Once submitted, the Sponsor will review your responses. If your site meets the initial requirements for the study, a representative from the Sponsor or their CRO will contact you directly regarding the next steps, such as a Site Selection Visit (SSV).
WHO DO I CONTACT WITH QUESTIONS ABOUT THE STUDY OR QUESTIONNAIRE?
The email you received should include a protocol synopsis for the study that should contain all the information you need to know about the study. If you still have questions about the protocol, or about the questionnaire, please use the contact form on this page or email support@ryght.ai.
How to Complete The Feasibility Questionnaire
1. Review the attached protocol synopsis
Review the disclosed or redacted protocol synopsis included in the original email to familiarize yourself with the study protocol.
Select the link in your email to view the feasibility questionnaire
The email you received contains a secure, unique link to the feasibility questionnaire for your site.
Invite colleagues to contribute to the questionnaire
Share the questionnaire with others at your site that are better suited to answer the questions if needed.
Answer study-specific questions
The questionnaire includes questions specific to this trial's requirements, such as patient population availability, equipment, and investigator interest.
Submit your response
Once you've reviewed and completed all sections, click "Submit." Your responses are immediately transmitted to the sponsor or CRO.
Most sites complete the questionnaire in 5-10 minutes. Traditional feasibility questionnaires typically take 2-4 hours to complete, making this experience much faster.
Get in Touch
If you would like to verify the authenticity of a specific study invitation, or if you are experiencing technical difficulties, please complete the form below. A member of our Clinical Site Support team will respond within 24 hours.

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