The Performance-Based CRO

Cleaner Data.
Faster Results.
Real-Time Visibility.

Technology-powered clinical trials for emerging life sciences companies. Database lock in days, not months.

Trusted by innovative life sciences companies

Bubs Australia
Algernon Pharmaceuticals
Coologics
Modra Pharmaceuticals
TECLens
Florida International University
University of Kentucky
Garden of Life
What Our Partners Say

Sponsors and sites trust Validcare

Full-Service CRO

Our approach

Validcare delivers all CRO services, site operations, and technology from protocol finalization through database lock—powered by direct source data management.

Learn more
01

End-to-End

One partner from protocol to database lock. No stitching multiple technologies and vendors together, no finger-pointing when things go wrong. Design, recruitment, data collection, and delivery—all under one roof, with one accountable team.

02

An Expert Team

Experienced, smart, honest, critical-thinking team members who stay engaged throughout your trial. Hands-on executive involvement—from protocol optimization and site planning to regulatory submission.

03

Tech-Enabled

SmartSource™ captures study data directly from the investigator or patient—eliminating transcription, reducing queries, and accelerating database lock. One unified platform for consent, data collection, monitoring, AE and PV management, and reporting.

Expect More From Your CRO

Data Quality
Significantly Fewer

Database Queries

Direct source data capture eliminates transcription errors and expensive SDV burden that slows traditional trials.

Transparency
No Surprises

On Budget and Milestones

Optimized operations and risk-monitoring dashboards increase visibility and reduce change orders.

Speed
Days or Weeks

From LPLV to Database Lock

Continuous data cleaning throughout your study means database lock in days or weeks—not months.

What is the Validcare Full-Service CRO?

A clinical trial is only as strong as its weakest link. With vertical integration and direct source data capture, Validcare acts as a single accountable partner for all your trial needs.

Capability Validcare Traditional CRO Clinical Tech Vendor Recruitment Vendor
Trial Management End-to-end project management
eClinical Platform SmartSource™ includes EDC, CTMS, ePRO, eTMF, and more Multiple Required
Direct Source Data Capture Eliminates SDV and significantly reduces queries
Site Network Internal and external sites for single and multi-site trials
Patient Recruitment Integrated digital recruitment and screening Partial
Performance-Based Contracts Fixed pricing, transparent pass-throughs, risk-sharing options
Real-Time Sponsor Dashboards Live visibility into enrollment, data quality, and milestones Partial

Our clinical research organization operates internationally

With legal presence in the United States, United Kingdom, Germany, Australia, Israel, Turkey, Poland, and Czechia—and operational reach across 40+ countries—we meet your study needs wherever patients are.

Legal presence
Operational reach
8 Legal entities
40+ Countries
Americas 6 countries
Legal presence: USA
Operational: Canada, Argentina, Brazil, Chile, Mexico
Western Europe 8 countries
Legal presence: UK, Germany
Operational: France, Italy, Spain, Switzerland, Netherlands, Portugal
Central-Eastern Europe 13 countries
Legal presence: Poland, Czechia
Operational: Austria, Baltic States, Bulgaria, Croatia, Greece, Hungary, Montenegro, Romania, Serbia, Slovakia, Slovenia
Nordic Countries 4 countries
Operational: Finland, Sweden, Norway, Denmark
Asia Pacific 7 countries
Legal presence: Australia
Operational: New Zealand, Japan, Philippines, Singapore, Malaysia, Taiwan
MENA Region 3 countries
Legal presence: Israel, Turkey
Operational: Lebanon
Africa 1 countries
Operational: South Africa
Let's Talk

Are you ready for an exceptional CRO experience?

Let's discuss your trial. We'll show you how the Validcare approach delivers faster, cleaner results—with pricing aligned to your success.

Include details about your therapeutic area, patient population, and timeline.