Provider profile

Medpace.

Clinical biometrics

Medpace describes itself as a global full-service CRO and documents biostatistics and data management, including CDASH-based CRF design, EDC including its own ClinTrak, medical coding, CDISC-standard databases, analysis plans, SAS-based analysis, DMC and interim analysis support and adaptive design advice. It lists a corporate address in Cincinnati, Ohio and offices across North America, Europe and Asia.

Website: medpace.com (opens in a new tab)
Sources reviewed: November 3, 2026 · Source pages re-checked within 4 months
First published: November 3, 2026

This profile summarizes what public sources state about the provider, mostly its own website. It is not an audit, qualification or endorsement by ArgusBio. Confirm capabilities directly with the provider before contracting.

Services and capabilities

Adaptive and Bayesian design1
Biostatistics1
CDISC data standards1
Clinical data management1
Data monitoring committee support1
EDC and database build1
Medical coding1
Statistical analysis plans1
Submission data packages1

Platforms and methods

SAS1

Engagement model

Full-service3,4

Development experience

Therapeutic experience

Cardiovascular2
Dermatology2
Gastroenterology and hepatology2
Hematology2
Immunology and inflammation2
Infectious diseases2
Metabolic and endocrine2
Nephrology2
Neuroscience / CNS2
Oncology2
Ophthalmology2
Pediatrics2
Rare diseases2
Respiratory2

Locations

Cincinnati, United States · Headquarters3Corporate address given in the site footer
Leuven, Belgium · Office4
Munich, Germany · Office4
Navi Mumbai, India · Office4
Tokyo, Japan · Office4
London, United Kingdom · Office4
Irving, United States · Office4Listed by the company as its Dallas office

Quality and regulatory

No quality framework or accreditation is established from reviewed sources. Ask for current certificates and recent inspection history.

Unknowns and questions to ask

Public sources rarely establish what matters most for a specific project. Confirm directly:

Named statistician and programming lead for your study, and their recent experience in your indication
Current capacity and realistic start date for database build and SAP authoring
Which CDISC standard versions and FDA Data Standards Catalog requirements they will deliver against
EDC system(s) supported and who holds the licence
Assumptions behind the budget: number of TLFs, interim analyses, DMC meetings and data transfers
How change orders are triggered and priced

Not established from reviewed sources: development stage, quality frameworks (vendor-reported).

How to choose a clinical biometrics CRO for a Phase 2 trial

Evidence and sources

1Biostatistics & Clinical Trial Data Management | Medpace CRO (opens in a new tab)Medpace · Provider website · retrieved November 3, 2026 · last checked November 3, 2026
2Therapeutic Clinical Development Expertise | Medpace (opens in a new tab)Medpace · Provider website · retrieved November 3, 2026 · last checked November 3, 2026
3Medpace page: medpace.com/about (opens in a new tab)Medpace · Provider website · retrieved November 3, 2026 · last checked November 3, 2026
4Global Office Locations | Medpace (opens in a new tab)Medpace · Provider website · retrieved November 3, 2026 · last checked November 3, 2026

“Last checked” means we confirmed the page was still available and still contained the cited statement. It does not mean ArgusBio verified the provider or its capabilities.

Something out of date or wrong? Request a correction. Corrections are reviewed against public sources before publication.

Contact

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