Clinical Trial Recruitment Services
Help people reach a clearer study conversation.
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Public Study Information and Site Handoffs
Start a Conversation
Clinical Trial Recruitment Services
Build a defined route from interest to your site.
A public listing can create interest, but people still need to understand what the study involves and whom to contact. Fanoni helps people explore source-linked trial information and prepare questions for the study team.
Discuss a possible collaboration around study awareness and administrative handoffs. Each program needs an agreed audience, contact route, service scope and review process before work starts.
Useful information. An agreed handoff. Site-led screening.
Public Study Record
Patient Questions
From the Question to the Next Step
Make each handoff easier to understand.
Review the Published Study
Use public registration details, listed requirements and locations as a starting point. Confirm recruiting status and site availability with the responsible team.
Agree the Inquiry Route
Define what information is needed, who receives the inquiry and how permission is recorded. Patient records need a separately approved channel.
Plan Administrative Follow-Up
Discuss support for unanswered practical questions, calls and visit communication. Confirm the steps Fanoni can support and the steps your site owns.
Your sites retain the clinical decisions.
Published requirements do not establish eligibility. The site performs screening, obtains informed consent and makes enrollment decisions under the protocol.
We do not promise qualified leads, referral volumes or faster enrollment. Begin with one workflow that your program and site teams can review.
Review Study Details
Define the Audience
Agree Site Contacts
Confirm Follow-Up
Questions Before Your Next Step
Does Fanoni pre-screen or enroll patients?
No automated clinical screening or enrollment service is represented here. Public trial exploration helps people prepare questions. Sites perform protocol screening, informed consent and enrollment.
Can you guarantee qualified leads?
No. A program needs a defined agreement, and clinical eligibility remains a site decision. No referral or enrollment volume is guaranteed.
Can a CRO inquire on behalf of a sponsor?
Yes. Send a general business inquiry and explain your organization and role in the program. Program authority and responsibilities need to be agreed separately.
Can this connect to our EHR or CTMS?
No live EHR or CTMS integration is offered by this website. Any future data exchange or integration requires a separately approved implementation.
Can I send patient records here?
No. Keep your inquiry general. Do not send patient names, health records or identifiable case details. Any later clinical-data exchange needs separate permissions and an approved channel.
Does this form create a partnership or book a call?
No. It is an initial inquiry for the Fanoni team to review. Submitting this form does not book an appointment or create an account. Any partnership or service delivery requires a separate agreement.
How could a recruitment collaboration begin?
Identify the study and locations, the questions patients need answered, who handles screening and how updates are shared. Confirm the operational scope before recruitment activity begins.
Sources and Further Reading
These sources provide background. They do not endorse Fanoni or confirm access to a provider or study.
Speak With Fanoni
Discuss your recruitment workflow.
Tell us the public study reference, relevant geography and the handoff you want to improve. Do not include identifiable patient information.
Program Inquiry
Your inquiry is saved in Fanoni’s private website inbox for the team to review. Keep your request general and do not include patient or medical details.
