Structured, privacy-aware support for sponsors, CROs, and sites — from patient identification through qualified referral.
Trialsolve does not make independent clinical decisions, does not replace site professional responsibilities, and does not claim that participation in a trial provides therapeutic benefit.
Patient-first approach
We build protocol-specific patient-facing landing pages in Hungarian — designed to explain the study clearly and guide eligible patients through a pre-screening questionnaire before any site contact.
Every patient interaction is guided by transparency and respect. Our coordinators explain study requirements in plain Hungarian, answer questions honestly, and never apply pressure.
Trialsolve aims to support clinical trial patient recruitment with transparent, well-documented, and locally-adapted solutions. We tailor our services to the study's objectives, target population, and approved processes, working in collaboration with sponsors, CROs, and sites.
We help define target groups, patient journey logic, pre-screening points, and anticipated enrollment challenges, so recruitment builds on realistic foundations from the planning stage.
We support the intake, documentation, and forwarding of patient inquiries to sites according to agreed roles and data processing rules.
Hungarian-language operations built on local market characteristics that can facilitate communication, streamline patient pathways, and align with sites.
We track campaign and funnel performance in a transparent way, so sponsors and partners get a clear picture of inbound interest, pre-screening rates, and process improvement opportunities.
Every engagement follows the same defined process. Your study team retains full control at every stage.
We understand the study objectives, inclusion logic, geographic focus, and operational constraints.
We design the proposed patient recruitment and pre-screening model, key communication elements, and operational responsibilities.
Patient communication materials and processes are aligned with required approval and data processing requirements. Clinical trial recruitment communication may be subject to ethical oversight, so patient-facing claims must be restrained and precise.
We support patient journeys from first contact to appropriate site referral through agreed channels.
We measure results, identify bottlenecks, and propose process refinements.
Whether you are running the study, managing the site, or overseeing the CRO, Trialsolve fits into your existing workflow.
Legal & Ethical Note: Trialsolve is not a healthcare provider, does not provide medical advice, and does not guarantee clinical trial enrollment. Participation decisions are always made by the appropriate site and study process under approved professional and ethical conditions.
If you're a sponsor, CRO, or site seeking patient recruitment, pre-screening, or local coordination support in Hungary, Trialsolve is ready to collaborate on a structured, transparent, and compliance-focused solution.
Confidential. Data processed per our Privacy Notice.