Clinical Trials & Patient Studies

Clinical Trial Travel, Simplified.

Compliant, confidential, and participant-centered travel support for sponsors, CROs, and study sites worldwide.

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Why Clinical Travel Is So Complex

Clinical study travel comes with challenges that most travel tools can’t solve:

  • Strict confidentiality and study blinding

  • Multiple sites and international participants

  • Regulatory and audit requirements

  • Hybrid and decentralized study models


    Traditional travel tools simply aren’t built for clinical research.

Solution — A Neutral Clearing House

Tripsmarter acts as a secure, centralized hub connecting sponsors, site coordinators, and participants.

  • Secure data encoding (participant IDs)

  • Dual approvals (cost by sponsor + logistics by site)

  • Smart reporting — redacted for sponsors, full for coordinators

  • One audit-ready invoice

We handle every detail — with compliance at the core.

Why Sponsors Choose Tripsmarter

🔒 Confidential & Compliant

HIPAA, GDPR, and study-blinding safeguards built in.

💡 Simple & Transparent

One easy compliant invoice, no hidden fees.

🧭 Trusted & Experienced

Two decades of clinical-grade travel expertise.

🌍 Scalable & Flexible

From single-site pilots to global multi-site studies.


Our Secure, Step-by-Step Process

How We Keep Clinical Travel Simple — and Compliant


Every study has its own rules, budgets, and sensitivities. Our process protects confidentiality, ensures transparency, and keeps every step effortless for coordinators and participants.

1. Define – Establish study-specific guidelines, budgets, and workflows.


2. Encode – Assign participant IDs securely, ensuring blinded data integrity.


3. Approve – Costs approved by the sponsor; logistics approved by the site coordinator.


4. Support – Coordinate travel and provide expert white-glove participant support.


5. Invoice – One consolidated invoice with masked participant data for compliance.


6. Close – Sponsor makes one clean payment; the study’s travel cycle is complete.

Our workflow gives sponsors and sites full visibility, full compliance, and zero guesswork — from the first itinerary to final reconciliation.


Built for People. Backed by Compliance.

Every clinical study depends on people: participants, caregivers, coordinators, and researchers working together toward better outcomes.

We simplify every journey so they can stay focused on the purpose of the study — advancing research and improving lives.

Sponsors maintain oversight without ever accessing personal participant data.


Coordinators gain full visibility and responsive logistical support.


Participants experience care, confidentiality, and comfort throughout their travel.


Every itinerary is managed with security, auditability, and compliance built in from the start.

At Tripsmarter, we combine human care with enterprise-grade precision to deliver confidence, compliance, and peace of mind at every stage of the study.

Ready to Simplify Your Next Study?

We’d love to learn about your upcoming study and show how Tripsmarter can make participant travel seamless, secure, and stress-free.

Our team supports sponsors and sites with participant-centered logistics — bringing structure, visibility, and reliability to every study, worldwide.

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Simplifying clinical travel. Strengthening research.