CROScout

CROs in China

Contract research organizations headquartered in China

28 organizations


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

Asymchem Laboratories

Tianjin, China CDMO1000+ employees

Chinese CDMO providing pharmaceutical development and manufacturing services from drug discovery to commercialization, known as a long-term supplier to major pharmaceutical companies including Pfizer.

GMP FDA Registered ISO 9001API SynthesisFormulation DevelopmentStability Testing

Bellen Chemistry

Dalian, China CDMO201-500 employees

Chinese CDMO specializing in custom synthesis of building blocks, advanced intermediates, and reference compounds for global pharmaceutical R&D, with a catalog of over 40,000 compounds.

ISO 9001 ISO 14001API SynthesisMedicinal ChemistryHit-to-Lead Optimization

BioDuro-Sundia Shanghai

Shanghai, China Full Service1001-5000 employees

Shanghai campus of BioDuro-Sundia providing integrated discovery and development services including medicinal chemistry, DMPK, biology, and preclinical development for global biotech.

GLP Compliant GMP CompliantHit-to-Lead OptimizationMedicinal ChemistryStructure-Activity Relationships (SAR)

CR Medicon

Nanjing, China Full Service501-1000 employees

Nanjing-based clinical CRO and Pharmaron subsidiary providing one-stop clinical development services in China including regulatory affairs, clinical operations, pharmacovigilance, and bioanalysis.

GCP CompliantPhase I Clinical TrialsPhase II Clinical TrialsPhase III Clinical Trials

Caidya (formerly Dian Diagnostics CRO)

Shanghai, China Full Service1000+ employees

China-based global CRO providing full clinical development services from Phase I through IV with strong site networks across China, Korea, and Southeast Asia.

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

ChemPartner

Shanghai, China Specialty501-1000 employees

Shanghai-headquartered CRO/CDMO offering integrated drug discovery chemistry, biology, and biologics development services including ADC and recombinant protein production.

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

Covance (Shanghai) Laboratory

Shanghai, China Specialty201-500 employees

Labcorp Drug Development's Chinese laboratory providing preclinical safety assessment, bioanalytical services, and clinical trial support for NMPA regulatory submissions.

GLP AAALAC ISO 9001General ToxicologyPK/ADME StudiesSafety Pharmacology

Dizal Pharma

Suzhou, China Specialty201-500 employees

Chinese CRO-turned-biotech providing clinical development services with deep oncology expertise, operating a portfolio of discovery through Phase III programs in solid tumors and hematological malignancies.

GCP CompliantPhase I Clinical TrialsPhase II Clinical TrialsPhase III Clinical Trials

Evopoint Biosciences

Shanghai, China Specialty51-200 employees

Shanghai-based preclinical CRO providing in vivo pharmacology, toxicology, DMPK, and bioanalytical services with specialized PDX platforms for oncology drug development.

GLP Compliant AAALACEfficacy StudiesGeneral ToxicologyPK/ADME Studies

Frontage Laboratories (China)

Shanghai, China Testing Lab501-1000 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

GCT CRO

Shanghai, China Full Service51-200 employees

Shanghai-based specialised clinical CRO providing full clinical development services in China and APAC with expertise in navigating NMPA regulatory pathways for multinational pharmaceutical companies.

GCP CompliantPhase I Clinical TrialsPhase II Clinical TrialsPhase III Clinical Trials

Hande Biotech

Suzhou, China Specialty201-500 employees

Chinese CRO and CDMO offering integrated preclinical biology, in-vitro pharmacology, and early drug discovery services for domestic and multinational pharma clients.

ISO 9001 GLP CompliantHit-to-Lead OptimizationIn Vitro ScreeningCompound Profiling

Hangzhou Zhongmei Huadong Pharmaceutical

Hangzhou, China Full Service1000+ employees

Chinese pharmaceutical company providing contract research and clinical development services for pharmaceutical companies seeking NMPA approvals in China.

GCP Compliant GMPPhase I Clinical TrialsPhase II Clinical TrialsPhase III Clinical Trials

Joinn Laboratories

Suzhou, China Specialty1000+ employees

Chinese preclinical CRO providing GLP-compliant safety evaluation, pharmacokinetics, efficacy studies, and drug metabolism studies with comprehensive NHP and rodent capabilities.

GLP AAALAC ISO 9001General ToxicologyPK/ADME StudiesSafety Pharmacology

Medicilon

Shanghai, China Full Service1000+ employees

Chinese integrated drug discovery and development CRO providing medicinal chemistry, ADME/PK, pharmacology, toxicology, and CMC services from Shanghai operations.

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

Novotech Greater China

Shanghai, China Full Service201-500 employees

Greater China operations of Australian CRO Novotech, providing full-service clinical trial management across mainland China, Hong Kong and Taiwan with NMPA submission expertise.

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

Pharmaceutical Product Development (PPD) China

Beijing, China Full Service501-1000 employees

PPD's Chinese clinical operations providing Phase I-IV clinical development, regulatory strategy, and site management for multinational and domestic pharmaceutical companies in Greater China.

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

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

Porton Pharma Solutions

Chongqing, China CDMO1000+ employees

Chinese CDMO providing API development and manufacturing services including custom synthesis, process development, and commercial-scale production from multiple GMP-certified facilities.

GMP FDA Registered ISO 9001API SynthesisFormulation DevelopmentStability Testing

ShangPharma

Shanghai, China Specialty501-1000 employees

One of China's earliest chemistry-focused CROs offering integrated drug discovery, DMPK, and pharmaceutical development services globally.

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

Shanghai GeneChem

Shanghai, China CDMO201-500 employees

Leading Chinese gene therapy CDMO providing lentiviral, adenoviral, and AAV vector manufacturing services along with custom cell line development for preclinical and clinical-grade production.

GMP Compliant ISO 9001Cell & Gene Therapy ManufacturingFormulation Development

Sundia MediTech

Shanghai, China CDMO1000+ employees

Chinese CRO and CDMO providing drug discovery chemistry, DMPK, analytical services, and clinical trial manufacturing from Shanghai and Chengdu operations.

GMP ISO 9001Medicinal ChemistryAPI SynthesisFormulation Development

Tigermed (Hangzhou Tigermed Consulting)

Hangzhou, China Full Service1000+ employees

China's largest independent CRO providing comprehensive clinical development services from preclinical through post-marketing with operations across China, Asia, and globally.

GCP Compliant GLP ISO 9001IND Filing SupportPhase I Clinical TrialsPhase II Clinical Trials

Viva Biotech

Shanghai, China Specialty1000+ employees

Chinese CRO/CDMO providing integrated drug discovery services including structure-based drug design, medicinal chemistry, ADME/PK studies, and biologics development from Shanghai operations.

GLP ISO 9001Hit-to-Lead OptimizationStructure-Activity Relationships (SAR)Medicinal Chemistry

WuXi Biologics

Wuxi, China CDMO1000+ employees

Global biologics CDMO providing end-to-end solutions for biologics drug development and manufacturing including monoclonal antibodies, bispecific antibodies, ADCs, and cell and gene therapies.

GMP FDA Registered ISO 9001Cell & Gene Therapy ManufacturingFormulation DevelopmentFill-Finish Services

WuXi Clinical

Shanghai, China Full Service1000+ employees

Clinical division of WuXi AppTec providing end-to-end Phase I-IV clinical trial services across China and Asia with expertise in NMPA, FDA and EMA regulatory submissions.

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

WuXi STA

Shanghai, China CDMO1000+ employees

WuXi AppTec's pharmaceutical development and manufacturing arm providing API process development, formulation development, analytical services, and GMP manufacturing from China and US facilities.

GMP FDA Registered ISO 9001API SynthesisFormulation DevelopmentFill-Finish Services