Search CROs

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

Citeline provides clinical trial intelligence, planning, feasibility, patient engagement, and regulatory compliance solutions to pharmaceutical sponsors. The platform delivers benchmarking across 400k+ trials, site selection, protocol optimization, and disclosure management services.

• Bioanalysis
• Biomarker Assays
• Biostatistics & Statistical Programming

QPS provides integrated contract research and clinical services spanning bioanalysis, preclinical development, and early-to-late phase clinical trials across multiple therapeutic areas including oncology, dermatology, and women's health.

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

CDSCO-registered CRO with 25+ years of clinical trial experience across Phase I–IV studies in India. Specializes in site management, clinical operations, and regulatory affairs across diverse therapeutic areas.

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

Sacura specializes in clinical trial management and regulatory support for biotech and pharma companies, with expertise in complex international studies and late-stage preclinical-to-market development planning.

• Bioanalysis
• Biostatistics & Statistical Programming
• Clinical Operations

Full-service Phase 1 CRO specializing in early-stage clinical trials, bioequivalence/bioavailability studies, and human abuse potential assessments with state-of-the-art facilities in Toronto and in-house bioanalytical labs.

• Bioanalysis
• Biomarker Assays
• Central Laboratory Services

Svar Life Science offers CRO services including bioanalytical testing, biomarker discovery, and GMP QC testing, alongside diagnostic services and cell manufacturing capabilities.

• Bioanalysis
• Biostatistics & Statistical Programming
• Clinical Operations

Specialized preclinical CRO dedicated to obesity research, offering comprehensive animal models, pharmacokinetic/pharmacodynamic studies, bioanalysis, and safety assessment for anti-obesity drug development.

• Clinical Operations
• Data Management & eClinical
• Medical Writing

Vanguard Clinical is a contract research organization providing comprehensive clinical trial services including monitoring, data management, medical writing, regulatory affairs, and trial management to pharmaceutical and biotech sponsors.

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

V2 Clinical is a clinical consulting CRO offering expert services in clinical operations, regulatory support, medical writing, data management, biostatistics, and quality assurance to biotech companies.

• Clinical Trial Services
• Regulatory Affairs
• US FDA Regulatory Strategy

Dermatology-focused CRO providing integrated, turnkey solutions across non-clinical, clinical, and regulatory development from concept to commercialization.

• Analytical Method Development & Validation
• Bioanalysis
• Biomarker Assays

San Diego-based bioanalytical CRO specializing in assay development and analysis for mRNA, oligonucleotides, and large molecules across discovery through clinical development phases.

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

Specialized CRO focused on metabolic diseases (obesity, diabetes, MASLD/MASH, cardiovascular, chronic kidney disease) with two decades of expertise, a nationwide registry of 180,000+ participants, and full-service clinical development capabilities from Phase 1 through Phase 3.

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

Full-service CRO specializing in oncology clinical trials, from preclinical IND-enabling studies through Phase I–III trial management, with expertise in First-in-Human studies for new cancer therapies.

• Bioanalysis
• Biomarker Assays
• Biostatistics & Statistical Programming

Sapient provides multi-omics biomarker discovery services—proteomics, metabolomics, and cytokine profiling—paired with biocomputational analysis and real-world validation to support drug development decisions across all phases.

• Analytical Method Development & Validation
• Phase I Clinical Trials
• Phase II Clinical Trials

ReechPharma specializes in customized formulation development and drug delivery systems for preclinical and clinical stages, supporting biotech and pharma companies with formulation research, analytical services, and GMP manufacturing.

• Biologics (Monoclonal Antibodies)

Boutique biologics CDMO providing analytical method development, process development, and cGMP manufacturing for biotech clients from early research through Phase 3, backed by over 20 years of experience and state-of-the-art facilities.

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

Cytel provides data science and advanced analytics solutions across the drug development lifecycle, from discovery through commercialization, including clinical trial design, adaptive trial strategies, real-world evidence, and regulatory support.