CRO Finder

Rare Disease CROs

Contract research organizations with rare disease expertise

12 organizations found

Catalent

Featured
Somerset, NJ, USA CDMO

Global leader in drug delivery technologies and development solutions. Catalent provides formulation, development, and manufacturing services for pharmaceuticals, biologics, and consumer health products.

GMP FDA Registered ISO 9001

Charles River Laboratories

Featured
Wilmington, MA, USA Full Service

Global leader in providing preclinical and clinical laboratory services. Charles River offers early-stage discovery, safety assessment, and clinical support services to pharmaceutical and biotech companies worldwide.

GLP AAALAC ISO 9001 GCP Compliant

ICON plc

Featured
Dublin, Ireland Full Service

Global provider of outsourced development and commercialization services to the pharmaceutical, biotechnology, and medical device industries. ICON specializes in clinical research with operations across 53 countries.

GCP Compliant ISO 9001 ISO 27001

PPD (Thermo Fisher Scientific)

Featured
Wilmington, NC, USA Full Service

A leading global contract research organization acquired by Thermo Fisher Scientific. PPD provides comprehensive clinical development services including laboratory, data management, and regulatory services.

GLP GCP Compliant CLIA CAP

Parexel International

Featured
Durham, NC, USA Full Service

Global biopharmaceutical services company providing clinical research, regulatory consulting, and market access services. Parexel has supported the development of many blockbuster drugs.

GCP Compliant ISO 9001

Certara

Princeton, NJ, USA Specialty

Biosimulation and regulatory science company providing model-informed drug development, regulatory science consulting, and software solutions for the pharmaceutical industry.

ISO 9001

Covance Genomics Lab (LabCorp)

Seattle, WA, USA Testing Lab

Specialty genomics laboratory providing biomarker services, companion diagnostics, and genomic profiling for clinical trials. Part of LabCorp Drug Development.

CLIA CAP ISO 15189

Eurofins CDMO

San Diego, CA, USA CDMO

CDMO division of Eurofins providing process development, analytical development, and GMP manufacturing for biopharmaceutical products including monoclonal antibodies and recombinant proteins.

GMP FDA Registered ISO 9001

Medpace

Cincinnati, OH, USA Full Service

Scientifically-driven, global, full-service clinical CRO providing Phase I-IV clinical development services. Medpace is known for its therapeutic expertise and operational efficiency.

GCP Compliant CLIA CAP

Novotech

Sydney, Australia Specialty

Asia-Pacific specialist CRO providing full-service clinical development capabilities with deep expertise in the Asia-Pacific regulatory landscape.

GCP Compliant ISO 9001

Samsung Biologics

Incheon, South Korea CDMO

Leading CDMO providing end-to-end biopharmaceutical manufacturing services including cell line development, process development, and commercial manufacturing at massive scale.

GMP FDA Registered ISO 9001

Worldwide Clinical Trials

Research Triangle Park, NC, USA Full Service

Mid-size global CRO providing Phase I-IV clinical development services with expertise in CNS, cardiovascular, and metabolic disease therapeutic areas.

GCP Compliant ISO 9001