CROScout

Testing Lab CROs

Contract testing laboratories provide analytical, bioanalytical, and quality control testing services. They support method development, stability studies, and regulatory testing requirements.

58 organizations


Acculab Life Sciences

San Diego, CA, USA1-50 employees

Specialty bioanalytical and analytical CRO providing method development, validation, and sample analysis services for pharmaceutical and biotech companies pursuing FDA submissions.

GLP ISO 9001Bioanalytical TestingMethod Development & ValidationStability Testing

Accutest Research Laboratories

Navi Mumbai, India201-500 employees

Indian CRO providing Phase I BA/BE studies, bioanalytical testing, clinical pharmacology and early-phase research services with USFDA-inspected facilities in Navi Mumbai.

GCP Compliant GLP ISO 9001 FDA RegisteredPhase I Clinical TrialsBioanalytical TestingMethod Development & Validation

Agilent Dissolution CRO

Wilmington, DE, USA51-200 employees

Contract analytical laboratory providing USP dissolution testing, method development, and stability studies for solid oral dosage form characterization under FDA guidelines.

GMP Compliant ISO 17025Method Development & ValidationStability TestingRaw Material Testing

Agilex Biolabs

Adelaide, Australia51-200 employees

Australian bioanalytical CRO providing GLP-compliant LC-MS/MS and ligand binding assay services for pharmacokinetic, bioequivalence, and immunogenicity studies supporting global regulatory submissions.

GLP ISO 9001Bioanalytical TestingMethod Development & ValidationPK/ADME Studies

Aliri Bioanalysis

Colorado Springs, CO, USA51-200 employees

Specialist bioanalytical CRO combining LC-MS/MS, mass spectrometry imaging, and spatial biology platforms to support regulated discovery and clinical sample analysis.

GLP Compliant ISO 9001 FDA RegisteredBioanalytical TestingMethod Development & ValidationPK/ADME Studies

Altogen Labs

Austin, TX, USA51-200 employees

GLP-compliant preclinical CRO in Austin, Texas, offering 100+ validated xenograft efficacy models, IND-enabling toxicology, and RNAi therapeutic development services.

GLP CompliantEfficacy StudiesGeneral ToxicologyIn Vitro Screening

Alturas Analytics

Moscow, ID, USA51-200 employees

GLP-compliant bioanalytical CRO with 25+ years of LC-MS/MS and GC-MS/MS expertise supporting preclinical-to-clinical drug development from purpose-built facilities.

GLP ISO 17025 FDA RegisteredBioanalytical TestingMethod Development & ValidationPK/ADME Studies

Anapharm Bioanalytics

Quebec City, Canada201-500 employees

Canadian bioanalytical CRO providing GLP-compliant LC-MS/MS bioanalytical services, PK analysis, and method development for pharmaceutical and biotech sponsors.

GLP Compliant GCP CompliantBioanalytical TestingMethod Development & ValidationPK/ADME Studies

Aptia Group (formerly Cyprotex/Evotec)

Macclesfield, UK201-500 employees

European ADME and DMPK specialist CRO providing in vitro ADME screening, drug-drug interaction studies, and physicochemical profiling from Macclesfield and Watertown facilities.

GLP ISO 9001PK/ADME StudiesIn Vitro ScreeningCompound Profiling

Averica Discovery Services

Shrewsbury, MA, USA51-200 employees

Specialty preclinical CRO offering bioanalytical chemistry, in vitro ADME screening, physicochemical profiling, and metabolite identification for drug discovery programs.

GLP FDA RegisteredPK/ADME StudiesIn Vitro ScreeningCompound Profiling

BRT Laboratories

Baltimore, MD, USA11-50 employees

Virginia-based safety pharmacology CRO providing cardiovascular telemetry, respiratory, and CNS safety studies in rodent and non-rodent species.

GLP Compliant AAALAC AccreditedSafety PharmacologyGeneral ToxicologyPK/ADME Studies

Bayer CropScience Tox Lab

Monheim, Germany201-500 employees

Bayer's contract toxicology laboratory in Germany providing regulatory toxicology studies, ecotoxicology testing, and safety assessment services for agrochemical and pharmaceutical compounds.

GLP Compliant OECD CompliantGeneral ToxicologyGenetic ToxicologyReproductive Toxicology

BioAgilytix

Durham, NC, USA201-500 employees

Leading large molecule bioanalytical CRO specializing in ligand-binding assays, immunogenicity testing, flow cytometry, and biomarker analysis for biologics drug development.

GLP FDA Registered ISO 17025Bioanalytical TestingMethod Development & ValidationPK/ADME Studies

Burleson Research Technologies

Morrisville, NC, USA11-50 employees

Preclinical CRO specialising in immunotoxicology and immune safety assessment, offering in vivo and in vitro studies for pharma, biotech, and government clients.

GLP Compliant AAALAC Accredited FDA RegisteredGeneral ToxicologySafety PharmacologyGenetic Toxicology

Covance Basel

Basel, Switzerland201-500 employees

LabCorp Drug Development centre in Basel providing central laboratory services, companion diagnostics development, and specialised clinical testing for European pharma sponsors.

GLP Compliant GCP Compliant ISO 15189Bioanalytical TestingMethod Development & ValidationStability Testing

Covance Food Solutions (now Eurofins)

Madison, WI, USA1000+ employees

Leading analytical and testing laboratory providing stability testing, extractables and leachables, raw material testing, and method development for pharmaceutical and food industries.

GLP ISO 17025 FDA Registered GMPStability TestingMethod Development & ValidationExtractables & Leachables

Covance Genomics Lab (LabCorp)

Seattle, WA, USA201-1000 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

Coventry Biomedical

Coventry, UK51-200 employees

UK-based bioanalytical and pharmaceutical testing CRO providing LC-MS/MS, dissolution testing, and method validation services for generic and innovator pharmaceutical companies.

GLP ISO 17025Bioanalytical TestingMethod Development & ValidationStability Testing

Eurofins India

Bangalore, India501-1000 employees

Eurofins' Indian bioanalytical and pharmaceutical testing operations providing method validation, stability testing, and raw material analysis for pharmaceutical companies.

GLP ISO 17025 ISO 9001Bioanalytical TestingMethod Development & ValidationStability Testing

Eurofins Panlabs Discovery

Toulouse, France501-1000 employees

Eurofins Discovery division providing high-throughput in-vitro pharmacology screening, compound profiling, ADME assays, and bioanalytical services supporting drug discovery from target identification through lead optimization.

GLP ISO 9001 ISO 17025Hit-to-Lead OptimizationIn Vitro ScreeningCompound Profiling

Eurofins Scientific

Luxembourg City, Luxembourg1000+ 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

Eurofins Viracor

Lee's Summit, MO, USA201-500 employees

Specialty reference laboratory providing clinical trial testing services including infectious disease biomarker analysis, transplant diagnostics, and immunogenicity testing for clinical studies.

CLIA CAP ISO 9001Method Development & ValidationBioanalytical Testing

Frontage Laboratories (China)

Shanghai, China501-1000 employees

Chinese operations of Frontage Laboratories providing bioanalytical services, ADME/PK studies, and analytical chemistry from GLP-compliant laboratories in Shanghai and Suzhou.

GLP ISO 9001Bioanalytical TestingMethod Development & ValidationPK/ADME Studies

Halo Labs

Burlingame, CA, USA1-50 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

ICON BioPharma Leiden

Leiden, Netherlands201-500 employees

Netherlands-based bioanalytical centre of excellence providing large-molecule bioanalysis, immunogenicity, and cell-based assay services for biologics and biosimilar programmes.

GLP Compliant GCP CompliantBioanalytical TestingMethod Development & ValidationPK/ADME Studies

ICON Bioanalytical Labs

Whitesboro, NY, USA201-500 employees

ICON's dedicated bioanalytical division providing GLP-compliant small and large molecule bioanalysis, immunogenicity testing, and biomarker analysis from state-of-the-art laboratories.

GLP GCP Compliant CLIA CAPBioanalytical TestingMethod Development & ValidationPK/ADME Studies

ICON Bioanalytical Whitesboro

Whitesboro, NY, USA201-500 employees

Specialised bioanalytical laboratory in New York providing large-molecule bioanalysis, immunogenicity testing, and ligand-binding assay development for biologics programmes.

GLP Compliant GCP Compliant FDA RegisteredBioanalytical TestingMethod Development & ValidationPK/ADME Studies

Integrated Laboratory Systems

Research Triangle Park, NC, USA51-200 employees

North Carolina-based genetic toxicology CRO providing GLP-compliant Ames, micronucleus, chromosomal aberration, and comet assays for regulatory submissions.

GLP Compliant FDA RegisteredGenetic ToxicologyGeneral ToxicologyIn Vitro Screening

Intertek Pharmaceutical Services

London, UK1000+ 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

KCAS Bio

Shawnee, KS, USA201-500 employees

Leading bioanalytical CRO with 45+ years of experience supporting 315+ approved drugs, offering LC-MS, ELISA, flow cytometry, and immunogenicity assays.

GLP FDA Registered ISO 17025Bioanalytical TestingMethod Development & ValidationPK/ADME Studies

Keystone Bioanalytical

North Wales, PA, USA51-200 employees

Pennsylvania-based bioanalytical CRO providing GLP-compliant LC-MS/MS and ligand-binding assay services for PK, immunogenicity, and biomarker analysis.

GLP Compliant FDA RegisteredBioanalytical TestingMethod Development & ValidationPK/ADME Studies

Kymos Group

Cerdanyola del Valles, Spain201-500 employees

GLP/GMP-certified European bioanalytical and CMC CRO near Barcelona with four laboratories and 240 experts serving the full pharmaceutical product lifecycle since 2001.

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

Lotus Labs India

Bangalore, India51-200 employees

Bangalore-based Indian CRO offering Phase I bioequivalence, bioanalytical and early-phase clinical research services for domestic and international generic pharmaceutical companies.

GCP Compliant GLP ISO 9001Phase I Clinical TrialsBioanalytical TestingMethod Development & Validation

Microbiologics

Saint Cloud, MN, USA51-200 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, USA201-1000 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, USA201-1000 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

NorthEast BioLab

Hamden, CT, USA51-200 employees

Founder-led bioanalytical CRO providing GLP-compliant LC-MS, ELISA, and qPCR services for PK, immunogenicity, and biomarker assays for pharma and biotech.

GLP FDA Registered ISO 17025Bioanalytical TestingMethod Development & ValidationPK/ADME Studies

Novascreen Biosciences

Hanover, MD, USA51-200 employees

Drug discovery services company providing in vitro pharmacology screening, ADME profiling, and custom assay development for pharmaceutical and biotech companies.

GLP ISO 9001In Vitro ScreeningCompound ProfilingPK/ADME Studies

PT Equilab International

Jakarta, Indonesia51-200 employees

Jakarta-based Indonesian CRO and bioanalytical laboratory providing BA/BE studies, clinical trials, and analytical services for pharmaceutical companies seeking Indonesian regulatory approval.

GLP Compliant GCP Compliant ISO 17025Bioanalytical TestingPhase I Clinical TrialsMethod Development & Validation

Pace Analytical Life Sciences

Minneapolis, MN, USA201-500 employees

US-based contract analytical laboratory providing GMP/GLP method development, validation, stability testing, and extractables/leachables studies for pharmaceutical and biotech sponsors.

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

Pacific Bioanalytical

San Diego, CA, USA51-200 employees

Bioanalytical CRO providing GLP-compliant LC-MS/MS and ligand binding assay services for pharmacokinetic, bioequivalence, and immunogenicity sample analysis to support clinical trials.

GLP ISO 9001Bioanalytical TestingMethod Development & ValidationPK/ADME Studies

Pacific Bioanalytical Inc

San Diego, CA, USA51-200 employees

California-based bioanalytical CRO providing LC-MS/MS method development, validation, and sample analysis for PK/PD studies supporting IND and NDA submissions.

GLP Compliant FDA RegisteredBioanalytical TestingMethod Development & ValidationPK/ADME Studies

Pacific Biolabs

Hercules, CA, USA51-200 employees

Bioanalytical and testing laboratory in the San Francisco Bay Area providing biocompatibility testing, extractables and leachables, sterility, and analytical chemistry services for pharma and medical devices.

GLP ISO 17025 FDA RegisteredExtractables & LeachablesStability TestingMethod Development & Validation

Pacific Biolabs

Hercules, CA, USA51-200 employees

San Francisco Bay Area testing laboratory providing biocompatibility, extractables/leachables, sterility, and microbiology testing for medical devices and pharmaceutical products.

GLP Compliant ISO 17025Extractables & LeachablesStability TestingRaw Material Testing

Pacific GMP

Camarillo, CA, USA11-50 employees

California-based cGMP testing laboratory providing raw material testing, stability studies, extractables/leachables, and method development for pharmaceutical and biotech clients.

GMP Certified FDA Registered ISO 17025Raw Material TestingStability TestingExtractables & Leachables

Pharmalytics

Montreal, Canada51-200 employees

Montreal-based analytical CRO providing GMP method development, stability testing, and extractables/leachables analysis for pharmaceutical and biologics sponsors.

GMP Certified ISO 17025Method Development & ValidationStability TestingExtractables & Leachables

REPROCELL

Yokohama, Japan51-200 employees

Global preclinical and drug discovery CRO offering the world's largest catalog of human fresh tissue assays for efficacy, ADME, and safety testing in GLP-accredited labs across the US, UK, and Japan.

GLP Compliant ISO 17025In Vitro ScreeningEfficacy StudiesSafety Pharmacology

Resolian

Indianapolis, IN, USA201-500 employees

Specialist bioanalytical, biomarker, and analytical sciences CRO with 500+ experts providing FDA/EMA-inspection-ready regulated bioanalysis across the US, UK, and Australia.

GLP ISO 17025 FDA RegisteredBioanalytical TestingMethod Development & ValidationPK/ADME Studies

SGS Life Sciences Belgium

Mechelen, Belgium201-500 employees

SGS's Belgian life sciences hub providing bioanalytical testing, method validation, and quality control services for pharmaceutical and biotech clients from GLP/GMP-certified laboratories.

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

SGS SA

Geneva, Switzerland1000+ 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

SGS Vitrology

Glasgow, United Kingdom51-200 employees

Glasgow-based specialty virology and biosafety testing CRO providing viral clearance validation, adventitious agent testing, and mycoplasma testing for biologics manufacturers.

GLP Compliant GMP Certified ISO 17025Bioanalytical TestingMethod Development & ValidationRaw Material Testing

Sitec Labs

Hyderabad, India51-200 employees

Indian bioanalytical and clinical research laboratory providing BA/BE studies, pharmacokinetic analysis, and analytical method development for generic and innovative drug programs.

GLP Compliant GCP Compliant NABLBioanalytical TestingMethod Development & ValidationPK/ADME Studies

Stillmeadow

Sugar Land, TX, USA51-200 employees

Independent GLP preclinical CRO and testing laboratory in Sugar Land, Texas, covering mammalian toxicology, aquatic, environmental, and animal health studies since 1975.

GLP Compliant ISO 17025 AAALACGeneral ToxicologySafety PharmacologyGenetic Toxicology

Synlab Analytics & Services

Munich, Germany1000+ employees

European laboratory services provider offering central laboratory, bioanalytical, and diagnostic testing services for clinical trials across Phase I-IV with 40+ labs worldwide.

GLP ISO 15189 ISO 9001Bioanalytical TestingMethod Development & ValidationStability Testing

Techno Pharma Jordan

Amman, Jordan51-200 employees

Amman-based Jordanian CRO and pharmaceutical company providing bioequivalence studies, BA/BE clinical trials, and contract analytical services for MENA pharmaceutical markets.

GMP Compliant GLP CompliantBioanalytical TestingPhase I Clinical TrialsMethod Development & Validation

XenoBiotic Laboratories

Plainsboro, NJ, USA51-200 employees

New Jersey-based bioanalytical and ADME/DMPK CRO founded in 1987, providing clinical and nonclinical metabolism and pharmacokinetics services to pharma, biotech, and agrochemical industries.

GLP Compliant ISO 17025PK/ADME StudiesBioanalytical TestingMethod Development & Validation

Xenotech (Japan)

Osaka, Japan51-200 employees

Japanese preclinical ADME services company providing in vitro metabolism, transporter, and drug interaction studies using human and animal tissue preparations for drug development.

GLP ISO 9001PK/ADME StudiesIn Vitro ScreeningBioanalytical Testing

ZeClinics

Barcelona, Spain11-50 employees

Barcelona-based preclinical CRO pioneering zebrafish-based platforms for efficacy testing, safety pharmacology, and toxicity assessment of pharmaceutical and chemical compounds.

GLP CompliantIn Vitro ScreeningEfficacy StudiesSafety Pharmacology