For BioPharma, Sponsors and CROs

Bring the patient journey into your program planning.

Start a Conversation

For BioPharma, Sponsors and CROs

Start with the barrier you want to solve.

Finding a study is only one part of the patient journey. Understanding the information, reaching the right contact and keeping practical next steps clear can matter just as much.

Fanoni invites sponsors, contract research organizations and service partners to discuss a defined collaboration around public study information and care navigation. Recruitment collaborations need an agreed scope; expanded access, real-world data and access-platform services are proposed areas for development.

A defined research site handoff. Illustrative workflow: Clinical referrals require a separately approved workflow.

A useful collaboration begins with a clear patient need and an agreed owner.

01

Study Information

Make public study details easier to understand and discuss.
02

Program Scope

Confirm available services, permissions and responsibilities.

From the Question to the Next Step

Three conversations to start with.

Clinical Trial Recruitment

Explore how source-linked study information, patient questions and administrative handoffs could support your sites. Site teams retain screening, consent and enrollment decisions.

A defined research site handoff. Illustrative workflow: Clinical referrals require a separately approved workflow.
Explore expanded access questions. Illustrative workflow: Drug access depends on separate clinical and program decisions.

Expanded Access Planning

Discuss a proposed navigation role around physician-led access pathways. Fanoni does not currently operate an expanded access program or distribute investigational medicines.

Data and Workflow Design

Explore proposed real-world data and access-management workflows. Start with the purpose, governance and operational owners before discussing a service or platform.

Start with the research question. Illustrative workflow: This is a proposed service, not a live clinical data system.

Agree what success would mean.

Define the audience, geography, study or program and the practical barrier. Then review feasibility, contact permissions, handoff responsibilities, reporting and any fees.

Explore the proposed access management platform direction. A discussion does not activate a program or guarantee referrals, enrollment or access.

Define the Need

1

Review Feasibility

2

Agree the Scope

3

Plan the Handoff

4

Questions Before Your Next Step

Sponsor teams, CROs, research sites and relevant service partners can send a general organizational inquiry. Tell us the workflow you want to discuss.

Fanoni Care supports exploration of public research information. Organizational recruitment and coordination support require a separate availability review and agreement. Expanded access operations, clinical data services and an access management platform are proposed, not active services.

Treating clinicians make medical decisions. Research sites manage protocol screening, informed consent, enrollment and study visits. Fanoni does not replace those responsibilities.

Scope, responsibilities and any fees must be discussed and agreed before work starts. This page is not a fee schedule or a promise of paid referrals.

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.

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.

What is available for BioPharma partners today?

Fanoni invites a general discussion about trial information and navigation needs. Expanded access operations, real-world data services and an access management platform are proposed directions that require further development and agreement.

Speak With Fanoni

Tell us where the journey gets stuck.

Start with the research question. Illustrative workflow: This is a proposed service, not a live clinical data system.

Share your organization, the program area and the practical question. Keep this an initial business inquiry, without 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.

Keep this general. Do not include patient names, health records or other patient-identifying details. Maximum 1,000 characters.