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• Bioanalysis
• Biomarker Assays
• Biostatistics & Statistical Programming

PPD is a leading global contract research organization (CRO) and the clinical research business of Thermo Fisher Scientific.

• Clinical Trial Services
• GLP Toxicology
• Preclinical In Vitro Studies

Esco Aster is a vertically integrated CDMO and CRO delivering end-to-end contract solutions from process development and GMP manufacturing through clinical research, with specialized capabilities in vaccine production, cell therapy, plasmid DNA, extracellular vesicles, and GLP toxicology.

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

Full-service CRO headquartered in Cairo, Egypt, providing clinical research services across phases I–IV with regional expertise in MENA and Africa, including feasibility assessment and publication support.

• 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
• Medical Writing
• Regulatory Affairs

Pubrica delivers research design, manuscript writing, statistical analysis, and publication support services to academic researchers, pharmaceutical companies, and clinical research organizations with 20+ years of expertise.

• 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.

• Bioanalysis
• In Vivo PK / PD Studies
• LC-MS Bioanalysis (Small Molecule)

GLP-compliant bioanalytical CRO specializing in LC-MS/MS solutions for preclinical and clinical research, IND submissions, and new drug applications.

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

European-based full-service CRO supporting biotech and medtech companies from Phase I through Phase IV and market access, with 80+ senior clinical research associates across Europe and the USA.

• Biostatistics & Statistical Programming
• Cardiovascular & Metabolic Specialty Services
• Clinical Operations

Caidya is a global, full-service CRO delivering personalized clinical development solutions across all phases of clinical research.

• 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.

• Translational Research
• Cell Therapy
• Gene Therapy

StemExpress, now part of CGT Global, supplies biospecimens and cell processing services for research and clinical applications, including GMP-grade leukopaks, PBMCs, and custom cell isolations.

• Bioinformatics & Data Science
• Biomarker Assays
• Genomics & Sequencing Services

Sampled is a large-scale biorepository and analytical services provider offering sample storage, management, multiomics analysis, cellular services, and custom kitting for clinical trials and research studies.

• 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.

• 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

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.

• 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
• Phase I Clinical Trials

PharPoint is a US-based CRO specializing in Phase I–IV clinical trials with rapid biometrics timelines, delivering database locks within 5 days of last patient visit and topline results in 2 business days.

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

Exclusively focused CNS contract research organization running Phase I-III neuroscience trials, with driving simulation for assessing how medications affect driving safety. Offers clinical trial management, trial design, data management, biostatistics, and medical writing to sponsors.