Search CROs

• Clinical Operations
• Phase I Clinical Trials
• Phase II Clinical Trials

Ergomed is a specialized CRO with 25+ years of experience delivering oncology, rare disease, and complex clinical trial solutions across all phases globally, backed by a team of 100+ MDs and PhDs.

• Clinical Operations
• Phase I Clinical Trials
• Phase II Clinical Trials

Global full-service CRO founded in 2000, offering end-to-end clinical trial support across all phases with integrated clinical supply chain management, logistics, and strategic sourcing capabilities.

• Clinical Operations
• Phase I Clinical Trials
• Phase II Clinical Trials

ProRelix Research supports Phase 1–4 clinical trials across pharmaceutical, biotechnology, and medical device sectors, offering clinical trial project management, data management, and medical writing services in compliance with ICH and GCP principles across the US, India, Europe, and Australia.

• Clinical Trial Services

Largest full-service Australian CRO delivering quality clinical trials with globally accepted data across AU, NZ, North America, and Asia.

• Clinical Operations
• Phase II Clinical Trials
• Phase III Clinical Trials

MPREX is a contract research organization in Pune, India, specializing in clinical trials in dermatology and claim-substantiation studies for skin and hair care products, with laboratory testing for product efficacy and safety.

• Clinical Operations
• Medical Writing
• Regulatory Affairs

CovarsaDx provides full-service clinical research, regulatory consulting, and quality assurance for IVD and medical device trials, with expertise in FDA 510(k), De Novo, and PMA pathways.

• Clinical Operations
• Regulatory Affairs
• US FDA Regulatory Strategy

Critical Path Institute convenes pharmaceutical, government, patient, and academic organizations to optimize drug and medical product development through collaborative consortia, regulatory science initiatives, and clinical trial design optimization.

• In Vitro Pharmacology
• In Vivo Efficacy Models
• In Vivo PK / PD Studies

GemPharmatech develops and supplies genetically engineered mouse models (GEMMs) and preclinical research services using CRISPR/Cas9 and gene-editing technologies, with a library of 25,000+ mouse strains including KO/cKO, humanized, and immunodeficient models.

• Biostatistics & Statistical Programming
• Central Laboratory Services
• Clinical Imaging Core Lab

Full-service CRO specializing in clinical trial management, advanced medical imaging, dosimetry, and data management across oncology, dermatology, and radiopharmaceutical therapies.

• Clinical Operations
• Phase I Clinical Trials
• Phase II Clinical Trials

TruTechnologies delivers live data capture at the point of care for clinical trials, enabling sponsors to detect issues and resolve deviations in real time across 3,300+ sites in 60 countries.

• Biomarker Assays
• Discovery Research
• Immunology & Inflammation Services

Full-service drug discovery CRO specializing in cell and molecular biology, biochemistry, enzymology, biomarker development, immunology, and in vivo efficacy models from idea through IND.

• Biostatistics & Statistical Programming
• Clinical Operations
• Phase I Clinical Trials

Full-service CRO delivering clinical trial services across Asia Pacific, with 50+ years of cumulative experience managing Phase I–IV trials and expertise in oncology, cardiovascular, CNS, and infectious disease indications.

• Antibody-Drug Conjugate (ADC)
• Biologics (Other)
• Small Molecule

Ardena is an integrated CDMO and bioanalytical CRO specializing in advanced drug product development, nanomedicine, and bioanalysis for complex molecules including poorly soluble compounds, highly potent APIs, and controlled substances.

• Analytical Method Development & Validation
• Biomarker Assays
• Computational & In-Silico Drug Discovery

Boston-based CRO specializing in assay development and biochemical & cellular screening for early-stage drug discovery, from target validation through lead optimization.

• Genetic Toxicology
• GLP Toxicology
• In Vitro ADME / DMPK

GLP-compliant nonclinical CRO specializing in safety and toxicology testing across in silico, in vitro, and in vivo modalities, with 35+ years of experience and nearly 6,000 completed studies.

• Analytical Method Development & Validation
• Bioanalysis
• Discovery Research

Advanced preclinical CRO providing comprehensive drug and device development services including bioanalysis, GLP toxicology, pharmacodynamic modeling, and specialized testing for oncology, infectious disease, gene therapy, and synthetic biology programs.

• DART (Reproductive & Developmental Toxicology)
• GLP Toxicology
• In Vivo Efficacy Models

Europe-based preclinical CRO specializing in GLP-compliant toxicology, safety assessment, and efficacy testing for small molecules and biologics, with AAALAC accreditation and integrated translational research capabilities.