Full-service CRO capability
Contract research and bioanalytical lab services that support your drug development programme through its analytical stages.
Clinical Trials
Your full-service CRO and study support partner
MedValue's international infrastructure and dedication to responsive, personalised partnerships support your programme no matter how complex it becomes — from bioanalytical lab work to the day-to-day data and administration that keeps a study moving.
International infrastructure
US-based management with delivery teams offshore, so study workload can be covered across time zones and scaled with enrolment.
Personalised partnership
Responsive, named points of contact rather than a ticket queue — however complex the programme becomes.
Where we support your study
Engage a single workstream or the full set. Scope, turnaround times and reporting are agreed up front for each study.
01
Clinical Data Management Support
Trained offshore teams handle the high-volume data work behind a study, so your in-house scientists and monitors stay on the science.
- Case report form data entry and transcription from source documents
- Query handling, tracking and follow-up support
- Listings, reconciliation checks and status reporting
- Coverage that scales up for enrolment peaks and database lock
02
Bioanalytical Lab Services
MedValue's contract research and bioanalytical lab capability supports sponsors through the analytical stages of a drug development programme.
- Sample logging, tracking and chain-of-custody documentation
- Result data capture and transfer into sponsor systems
- Study documentation management and indexing
- Coordination between lab, sponsor and site teams
03
Site & Sponsor Administrative Support
Responsive, personalised partnership across the administrative load of running a trial — the work that quietly slows studies down.
- Regulatory and study binder document preparation and indexing
- Investigator and site document collection and tracking
- Meeting scheduling, minutes and correspondence support
- Study status dashboards and recurring reporting
04
Research Billing & Coverage Support
For provider-run research programmes, we keep study-related billing separate from routine care billing.
- Separation of study-funded and routine-care charges
- Charge capture support against the study budget
- Invoice preparation and reconciliation support for sponsors
- Reporting your finance and research teams can both read
AI clinical trials dashboard
A concept demo of study portfolio, enrollment and data-quality reporting in one view.
See the conceptEDI services
Paper claims to EDI conversion, enrollment processing and EOB-to-835 remittances.
See payer servicesProvider & practice services
Revenue cycle management, credentialing and enrollments, and billing assessments.
View servicesClinical trial support
Scope the study support your programme needs
Share your organization type, active studies and where you need help. Our clinical trials team responds with a support plan covering data, lab and administrative work.
- Clinical data management, entry and quality review
- Bioanalytical lab and study administration support
- Flexible teams that scale study by study
- Confidentiality and documented quality controls
Prefer to talk first? Call 630-430-1040
Request clinical trial support
Share your study profile and we'll scope the data, lab and administrative support your programme needs.