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Find the right research partner from 42 organizations


Catalent

Featured
Somerset, NJ, USA CDMO1000+ employees

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 9001Formulation DevelopmentFill-Finish ServicesPackaging & Labeling

Charles River Laboratories

Featured
Wilmington, MA, USA Full Service1000+ employees

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 CompliantGeneral ToxicologyPK/ADME StudiesEfficacy Studies

ICON plc

Featured
Dublin, Ireland Full Service1000+ employees

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 27001Phase I Clinical TrialsPhase II Clinical TrialsPhase III Clinical Trials

Labcorp Drug Development

Featured
Burlington, NC, USA Full Service1000+ employees

Formerly Covance, Labcorp Drug Development provides comprehensive drug development services from early discovery through post-approval. One of the world's largest CROs with extensive nonclinical and clinical capabilities.

GLP GMP AAALAC GCP CompliantGeneral ToxicologyPK/ADME StudiesSafety Pharmacology

Lonza

Featured
Basel, Switzerland CDMO1000+ employees

Leading CDMO providing custom development and manufacturing for the pharmaceutical and biotech industries. Lonza specializes in biologics, cell and gene therapy, and small molecule manufacturing.

GMP FDA Registered ISO 9001 ISO 14001API SynthesisFormulation DevelopmentFill-Finish Services

PPD (Thermo Fisher Scientific)

Featured
Wilmington, NC, USA Full Service1000+ employees

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 CAPPhase I Clinical TrialsPhase II Clinical TrialsPhase III Clinical Trials

Parexel International

Featured
Durham, NC, USA Full Service1000+ employees

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 9001Phase I Clinical TrialsPhase II Clinical TrialsPhase III Clinical Trials

Syneos Health

Featured
Morrisville, NC, USA Full Service1000+ employees

Integrated biopharmaceutical solutions company combining clinical development and commercial capabilities. Syneos offers end-to-end solutions from Phase I through product launch and beyond.

GCP Compliant ISO 9001Phase I Clinical TrialsPhase II Clinical TrialsPhase III Clinical Trials

WuXi AppTec

Featured
Shanghai, China Full Service1000+ employees

Leading global pharmaceutical and medical device open-access capability and technology platform. WuXi AppTec provides services spanning from discovery through manufacturing across small molecules, biologics, and cell/gene therapies.

GLP GMP AAALAC ISO 9001Hit-to-Lead OptimizationMedicinal ChemistryIn Vitro Screening

Absorption Systems (Pharmaron)

Exton, PA, USA Full Service1000+ employees

Preclinical ADME and pharmacokinetic service provider now part of Pharmaron. Specializes in in vitro and in vivo DMPK, drug transporter studies, and metabolite identification.

GLP AAALACPK/ADME StudiesGeneral ToxicologySafety Pharmacology

Altasciences

Laval, QC, Canada Full Service201-1000 employees

Mid-size CRO offering early-phase clinical studies, preclinical safety assessment, and bioanalytical services. Known for integrated PK/PD programs from preclinical through Phase I.

GLP GCP Compliant AAALAC CLIAGeneral ToxicologyPK/ADME StudiesSafety Pharmacology

Aptuit (Evotec)

Verona, Italy Full Service201-1000 employees

Integrated drug discovery and development services company now part of Evotec. Provides ADME/DMPK, safety assessment, and pharmaceutical development services.

GLP GMP ISO 9001PK/ADME StudiesGeneral ToxicologySafety Pharmacology

Celerion

Lincoln, NE, USA Specialty201-1000 employees

Specialized early clinical research CRO providing Phase I clinical pharmacology, bioanalytical, and ADME services from dedicated clinical units.

GLP GCP Compliant CLIA CAPPhase I Clinical TrialsBioanalytical TestingPK/ADME Studies

Certara

Princeton, NJ, USA Specialty201-1000 employees

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

ISO 9001Regulatory StrategyIND Filing SupportNDA/BLA Support

Champions Oncology

Hackensack, NJ, USA Specialty51-200 employees

Specialty CRO focused on translational oncology services. Champions provides patient-derived xenograft (PDX) tumor models, ex vivo tumor platforms, and oncology pharmacology studies.

GLP AAALACEfficacy StudiesIn Vitro ScreeningCompound Profiling

Covance Genomics Lab (LabCorp)

Seattle, WA, USA Testing Lab201-1000 employees

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

CLIA CAP ISO 15189Bioanalytical TestingMethod Development & Validation

Crown Bioscience

San Diego, CA, USA Specialty201-1000 employees

Translational oncology and metabolic disease CRO providing tumor models (PDX, syngeneic, humanized), oncology pharmacology, and biomarker services for drug discovery.

AAALAC GLPEfficacy StudiesIn Vitro ScreeningCompound Profiling

Envigo (Inotiv)

Indianapolis, IN, USA Specialty1000+ employees

Research models and services provider offering genetically defined laboratory animals, contract research services, and scientific consulting for preclinical drug development.

GLP AAALACGeneral ToxicologyEfficacy StudiesGenetic Toxicology

Eurofins CDMO

San Diego, CA, USA CDMO201-1000 employees

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 9001Formulation DevelopmentFill-Finish ServicesMethod Development & Validation

Eurofins Scientific

Luxembourg City, Luxembourg Testing Lab1000+ employees

International group of laboratories providing testing and support services to the pharmaceutical, food, environmental, and consumer products industries. Major provider of bioanalytical and analytical testing services.

GLP GMP ISO 17025 CLIABioanalytical TestingMethod Development & ValidationStability Testing

Evotec

Hamburg, Germany Specialty1000+ employees

Drug discovery and development company offering a range of discovery and preclinical services including target validation, hit identification, lead optimization, and ADME/PK.

GLP ISO 9001Hit-to-Lead OptimizationStructure-Activity Relationships (SAR)In Vitro Screening

Frontage Laboratories

Exton, PA, USA Full Service201-1000 employees

CRO providing integrated drug discovery and development services including ADME/PK, bioanalytical, CMC, and clinical services with operations in the US and China.

GLP GMP CLIA FDA RegisteredPK/ADME StudiesBioanalytical TestingMethod Development & Validation

Halo Labs

Burlingame, CA, USA Testing Lab1-50 employees

Analytical services CRO specializing in subvisible particle characterization, aggregation analysis, and container closure integrity testing for biologics and pharmaceutical products.

ISO 17025Method Development & ValidationStability TestingExtractables & Leachables

Inotiv

West Lafayette, IN, USA Full Service1000+ employees

Contract research organization providing drug discovery and development services including preclinical safety assessment, bioanalytical services, and research animal models.

GLP AAALAC ISO 9001General ToxicologyPK/ADME StudiesSafety Pharmacology

Intertek Pharmaceutical Services

London, UK Testing Lab1000+ employees

Global testing and certification provider offering comprehensive pharmaceutical services including analytical testing, stability studies, extractables/leachables, and regulatory consulting.

GLP GMP ISO 17025 FDA RegisteredMethod Development & ValidationStability TestingExtractables & Leachables

Medpace

Cincinnati, OH, USA Full Service1000+ employees

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 CAPPhase I Clinical TrialsPhase II Clinical TrialsPhase III Clinical Trials

Microbiologics

Saint Cloud, MN, USA Testing Lab51-200 employees

Quality control reference material provider and testing laboratory serving pharmaceutical, medical device, and clinical diagnostics industries with microbiology standards.

ISO 17025 ISO 13485 FDA RegisteredRaw Material TestingMethod Development & Validation

NAMSA

Northwood, OH, USA Testing Lab201-1000 employees

Leading medical device CRO providing biocompatibility testing, sterilization validation, regulatory consulting, and clinical services for medical device and combination product development.

GLP ISO 17025 ISO 13485 FDA RegisteredGeneral ToxicologyExtractables & LeachablesStability Testing

Nelson Laboratories (Sotera Health)

Salt Lake City, UT, USA Testing Lab201-1000 employees

Premier provider of sterilization validation, microbiology, and biocompatibility testing services for medical devices. Part of Sotera Health, serving the global healthcare industry.

GLP ISO 17025 ISO 13485 FDA RegisteredExtractables & LeachablesStability TestingRaw Material Testing

Novascreen Biosciences (Calvert Labs)

Scott Township, PA, USA Specialty51-200 employees

Preclinical CRO specializing in in vitro pharmacology, receptor binding, enzyme inhibition assays, and ADME screening for drug discovery programs.

GLP AAALACGeneral ToxicologyPK/ADME StudiesSafety Pharmacology

Novotech

Sydney, Australia Specialty201-1000 employees

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

GCP Compliant ISO 9001Phase I Clinical TrialsPhase II Clinical TrialsPhase III Clinical Trials

PRA Health Sciences (ICON)

Raleigh, NC, USA Full Service1000+ employees

Global CRO acquired by ICON in 2021. Provides full-service clinical development, data management, and strategic consulting across all major therapeutic areas.

GCP Compliant ISO 9001Phase I Clinical TrialsPhase II Clinical TrialsPhase III Clinical Trials

Pacific Biotech

San Francisco, CA, USA Specialty51-200 employees

Specialty preclinical CRO focused on Asia-Pacific markets, providing preclinical safety assessment, pharmacology, and bioanalytical services for small molecule and biologic programs.

GLP ISO 17025General ToxicologyEfficacy StudiesExtractables & Leachables

Pharmaron

Beijing, China Full Service1000+ employees

Integrated pharmaceutical R&D service platform offering drug discovery, preclinical, clinical, and commercial manufacturing services to biotech and pharma companies globally.

GLP GMP AAALAC FDA RegisteredHit-to-Lead OptimizationMedicinal ChemistryIn Vitro Screening

Phibro Animal Health / SAFC

Ashland, OH, USA Specialty201-1000 employees

Preclinical CRO providing GLP-compliant safety assessment services including general toxicology, developmental and reproductive toxicology, and carcinogenicity studies.

GLP AAALACGeneral ToxicologyReproductive ToxicologyCarcinogenicity Studies

QPS

Newark, DE, USA Full Service201-1000 employees

Global CRO providing bioanalytical, clinical pharmacology, and Phase I-IV clinical trial services. QPS operates CLIA-certified bioanalytical laboratories supporting regulated studies.

GLP GCP Compliant CLIA CAPBioanalytical TestingMethod Development & ValidationPhase I Clinical Trials

Reaction Biology

Malvern, PA, USA Specialty51-200 employees

Specialty CRO providing biochemical and cell-based assay services for drug discovery. Known for kinase profiling, epigenetic screening, and custom assay development.

ISO 9001In Vitro ScreeningCompound ProfilingTarget Validation

Recipharm

Stockholm, Sweden CDMO1000+ employees

Leading CDMO providing pharmaceutical manufacturing services including development, scale-up, and commercial production of oral solids, sterile products, and complex formulations.

GMP FDA Registered ISO 9001 ISO 14001Formulation DevelopmentFill-Finish ServicesPackaging & Labeling

SGS SA

Geneva, Switzerland Testing Lab1000+ employees

World's leading testing, inspection, and certification company. SGS provides pharmaceutical analytical services, clinical research, and regulatory compliance testing globally.

GLP GMP ISO 17025 ISO 9001Bioanalytical TestingMethod Development & ValidationStability Testing

Samsung Biologics

Incheon, South Korea CDMO1000+ employees

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 9001Formulation DevelopmentFill-Finish ServicesCell & Gene Therapy Manufacturing

Worldwide Clinical Trials

Research Triangle Park, NC, USA Full Service201-1000 employees

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

GCP Compliant ISO 9001Phase I Clinical TrialsPhase II Clinical TrialsPhase III Clinical Trials

Xenotech (Sekisui XenoTech)

Kansas City, KS, USA Specialty51-200 employees

Specialty ADME/PK CRO providing in vitro and in vivo drug metabolism and pharmacokinetic studies. Known for comprehensive ADME characterization using human and animal tissues.

GLP ISO 9001PK/ADME StudiesIn Vitro ScreeningCompound Profiling