For sponsors and CROs
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.
Accelerate Phase 1–4 study startup with high-capacity independent investigative sites vetted for equipment, patient velocity, and PI track record.
Submit protocol criteria and receive an aggregated multi-site feasibility packet within 48 hours containing verified PI CVs, equipment audits (-80°C freezers, centrifuges), and local epidemiology.
Corterve charges sponsors zero placement or brokerage markups. Participating sites engage Corterve for external BD and startup administrative enablement directly.
Fully compliant with 42 U.S.C. § 1320a-7b and 18 U.S.C. § 220 (EKRA). Zero per-patient bounties, non-delegated Form FDA 1572 responsibilities, and central IRB velocity.
Community access becomes a handoff your investigators can accept or close. Illustrative study-team view.
Study-team inbox
Study teams decide eligibility and enrollment. We take on the finding.
Corterve helps sponsors reach people who may be new to research through community engagement rather than recycled vendor lists. Community outreach connects real people in local settings with study teams for independent evaluation.
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.
Participants reached through community settings, not reused recruitment databases. Sourcing focuses on community outreach rather than purchased advertising 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.
Consent-first records of how someone was introduced, for the study team to review. We do not determine eligibility.
Community engagement, consented introductions, and optional field materials. No unpublished SKUs and no promised enrollment outcome.
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
Reach people who have not been recycled through digital ads. Consented introductions go to study teams for review.
Sponsors and CROs
Order branded field materials for your community presence — with fulfillment included.
Sponsors, CROs, and research sites
Our design team prepares branded materials so your team can focus on community conversations, not layout tools.
Sponsors, CROs, and research sites
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 CallTell us about reaching people for your studies. The right person will reply.
Encrypted in transit and at rest. Shared with a study team only after consent. Read what we claim.
Privacy-by-design practices aligned to HIPAA requirements. Code evidence — not a certification.
Patient data encrypted in transit and at rest across all platform surfaces.
No patient information is shared without explicit, informed consent.
