Search CROs

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

Clinilabs is the leading CNS-focused CRO with 25+ years of expertise in neurotherapeutic clinical trials, offering Phase 1–4 trial management, early-phase development, clinical research units, and MedTech device expertise across psychiatry, neurology, substance use, and rare CNS disorders.

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

Data-focused CRO providing full-spectrum biometrics, regulatory submissions, safety & risk management, and therapeutic expertise across oncology, CNS, rare diseases, and psychedelics. Named Best Specialist CRO at the Scrip Awards with zero refusals to file on 50+ marketing applications in five years.

• Biostatistics & Statistical Programming
• Clinical Operations
• Data Management & eClinical

Veridix is the eClinical and AI technology platform of Emmes Group, providing modernized electronic data capture, decentralized trial solutions, and AI-powered agents for clinical data management and biostatistics to support Phase I–IV trials across 90+ countries.

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

Medidata provides a unified clinical trial platform with AI-driven data management, electronic data capture, patient engagement tools, and real-world data integration to accelerate research across all trial phases.

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

Global CRO delivering clinical trial management, regulatory consultancy, data management, and medical writing for biotech, pharma, and medical device companies across Phase I–IV studies and real-world evidence programs.

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

Full-service preclinical and clinical CRO supporting pharmaceutical, biotechnology, and medical device companies with trial design, site selection, data management, statistical analysis, and medical writing across Asia-Pacific.

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

ISO 9001:2015-certified CRO offering end-to-end clinical research services including Phase I–IV trials, medical writing, biostatistics, data management, and regulatory support across pharmaceuticals, nutraceuticals, devices, and biotech.

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

Indian CRO providing end-to-end clinical trial services (Phase I–IV), regulatory support, medical writing, biostatistics, data management, and biospecimen procurement across pharmaceuticals, biologics, medical devices, and nutraceuticals.

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

European full-service CRO supporting clinical development from Phase I to IV and non-interventional studies, with expertise in clinical monitoring, data management, biostatistics, medical writing, and regulatory affairs.

• Cell Therapy
• Gene Therapy
• Radiopharmaceutical

Covance provides contract research, nonclinical testing, central laboratory services, and real-world data solutions to biopharma sponsors across oncology, cell and gene therapies, radiopharmaceuticals, vaccines, and precision medicine.

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

Clinical trial and strategic consulting CRO offering innovation-enabled trial solutions, digital training, patient engagement programs, and regulatory consulting across multiple therapeutic areas including oncology, CNS, cardiovascular, and rare disease.

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

ObvioHealth delivers decentralized and hybrid clinical trial solutions through its ObvioGo platform, enabling sponsors to simplify study design, boost participant engagement, and accelerate enrollment across 40 countries.

• Analytical Method Development & Validation
• ICH Stability Studies
• Biologics (Monoclonal Antibodies)

Global cGMP contract research organization providing comprehensive analytical services for drug development, from preclinical through commercialization, with expertise in biologics, cell & gene therapies, and small molecules.

• Bioanalysis
• Biomarker Assays
• Genomics & Sequencing Services

GLP- and GCLP-compliant molecular CRO specializing in bioanalysis for gene therapy, RNA therapeutics, and advanced modalities, offering qPCR, NGS, and plasma proteomics services since 2001.

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

Full-service CRO providing clinical trial management, regulatory consulting, pharmacovigilance, biostatistics, and medical writing across 40+ countries with AI-secure eClinical systems and patient-centered trial design.

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

CMIC HOLDINGS is a Japanese contract research and manufacturing organization providing end-to-end pharmaceutical solutions from non-clinical through post-marketing phases, including consulting, CRO, CDMO, and SMO services.

• Clinical Imaging Core Lab
• Clinical Operations
• Phase I Clinical Trials

Radiologist-founded oncology imaging CRO offering DICOM collect & hold, central reads by subspecialist radiologists, and AI-assisted volumetric analysis for Phase I/II trials. FDA 21 CFR Part 11, HIPAA, and GDPR compliant with 24–72 hour turnaround.

• Analytical Method Development & Validation
• Biostatistics & Statistical Programming
• Clinical Operations

Atheln provides customized strategic and operational consulting across product development, CMC, nonclinical, clinical, regulatory, and commercial services for pharma, biotech, and medtech clients.