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For sponsors and CROs

Diversified community access. Consented interest. Study teams decide.

Reach people who have not been recycled through digital ads. Introductions go to your study teams for review. Finding people is the work we take on.

What your study team reviews

A consented packet — not a score, not a quota

Community access becomes a handoff your investigators can accept or close. Illustrative study-team view.

Consented introduction

Study-team inbox

Introduction ready for review

Awaiting investigator decision
Sourcing
Community conversations — not recycled vendor lists
Consent
Recorded before any contact details moved
What we did
Found people who may be new to research and asked to be introduced
What we did not do
Determine eligibility, award a site, or promise an enrollment number

Study teams decide eligibility and enrollment. We take on the finding.

For Sponsors & CROs

Community-sourced introductions. Eligibility stays with the study team.

Corterve helps sponsors reach people who may be new to research through community engagement rather than recycled vendor lists. Trial-naive is a sourcing aim — a description of who we look for, not a guarantee about every introduction.

Consent-first introductions

A pathway a study team can review — not a path that ends in enrollment by default

Community engagement replaces purchased lists with consented introductions. People are brought to the study team for review. We do not determine eligibility and we do not describe a public lead-scoring engine.

Community-first sourcing

We look for people who have not been cycled through trial ads. Trial-naive is a sourcing aim — not a claim of lower placebo rates or cleaner signal.

People, not recycled lists

Introductions are meant to come from real community and clinical settings — not from recycled vendor databases. That is a sourcing description, not an enrollment result.

Documentation for review

Consent-first records of how someone was introduced, for the study team to review. We do not determine eligibility.

What we take on with you

Community engagement, consented introductions, and optional field materials. No unpublished SKUs and no promised enrollment outcome.

Local community engagement

We help sponsors reach people who may be new to research through community engagement, with a record a study team can review. Study teams decide who joins.

Sponsors and CROs

  • • Community engagement rather than recycled digital lists
  • • Consented introductions a study team can review
  • • Study teams decide eligibility and enrollment

Community Sponsorship

Reach people who have not been recycled through digital ads. Consented introductions go to study teams for review.

Sponsors and CROs

  • • Sourcing aim: people who may be new to research
  • • Documentation a study team can review
  • • No promised enrollment outcome

Field Materials

Order branded field materials for your community presence — with fulfillment included.

Sponsors, CROs, and research sites

  • • Consistent brand presence across every community engagement
  • • Your logo and brand colors on field materials
  • • Straightforward per-activation ordering

Design Support

Our design team prepares branded materials so your team can focus on community conversations, not layout tools.

Sponsors, CROs, and research sites

  • • Design requests tied to a specific community activation
  • • Brand assets auto-loaded from your org profile
  • • Review and approve before production
Sponsor & CRO conversations

Scoped community access for open protocols.

Study design, site conversations, and enrollment-risk discussions — scoped with your team. Finding people is the work we take on. Enrollment numbers stay with the study team.

Book an Exploratory Call

Book an Exploratory Call

Tell us about reaching people for your studies. The right person will reply.

The primary indication or disease area, if you have one.

When you need introductions to begin, if you know.

Do not send patient data

This channel is designated for strategic partnerships and feasibility inquiries. Do not submit patient-level data, Protected Health Information (PHI), or proprietary protocol datasets through this form. Use only non-sensitive business details here; we will follow up through approved channels if a secure exchange is needed.

How we handle information

Encrypted in transit and at rest. Shared with a study team only after consent. Read what we claim.

HIPAA-Aligned Architecture

Privacy-by-design practices aligned to HIPAA requirements. Code evidence — not a certification.

End-to-End Data Encryption

Patient data encrypted in transit and at rest across all platform surfaces.

Strict Consent-First Routing

No patient information is shared without explicit, informed consent.