CROScout

CROs in France

Contract research organizations headquartered in France

13 organizations


Aixial Group

Levallois-Perret, France Full Service1001-5000 employees

Mid-size global CRO under ALTEN Group formed by integrating Cmed and Larix, with deep oncology, rare disease, and cell/gene therapy clinical trial expertise across the US and Europe.

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

Astellia CRO

Lyon, France Full Service51-200 employees

French CRO providing Phase I-III clinical development services with particular expertise in metabolic disease, endocrinology, and cardiovascular trials across Europe.

GCP CompliantPhase I Clinical TrialsPhase II Clinical TrialsPhase III Clinical Trials

Astellia Pharma France

Paris, France Specialty11-50 employees

French CRO providing Phase I-III clinical trial management and monitoring services across France and Western Europe, with expertise in rare disease and orphan drug development.

GCP CompliantPhase I Clinical TrialsPhase II Clinical TrialsPhase III Clinical Trials

Atlanbio

Saint-Herblain, France Specialty11-50 employees

Nantes-based French CRO specialising in CNS, sleep medicine, and neuroscience clinical trials with proprietary EEG/PSG expertise and Phase I-II clinical pharmacology capabilities.

GCP CompliantPhase I Clinical TrialsPhase II Clinical TrialsClinical Data Management

Biotrial

Rennes, France Specialty201-500 employees

Transatlantic Phase 1 CRO with clinical pharmacology units in Rennes (France) and Newark (NJ, USA). Specializes in first-in-human, CNS, cardiac safety, and abuse liability studies.

GLP GCP Compliant ANSM ApprovedPhase I Clinical TrialsPK/ADME StudiesSafety Pharmacology

ERBC Group

Lyon, France Specialty51-200 employees

French preclinical CRO based in Lyon evaluating efficacy and safety of new compounds including drugs, biologics, and medical devices across innovative in-vitro and in-vivo models.

GLP GCP CompliantIn Vitro ScreeningEfficacy StudiesGeneral Toxicology

Eurofins Panlabs Discovery

Toulouse, France Testing Lab501-1000 employees

Eurofins Discovery division providing high-throughput in-vitro pharmacology screening, compound profiling, ADME assays, and bioanalytical services supporting drug discovery from target identification through lead optimization.

GLP ISO 9001 ISO 17025Hit-to-Lead OptimizationIn Vitro ScreeningCompound Profiling

Excelya Group

Paris, France Full Service501-1000 employees

Paris-based European CRO providing clinical operations, pharmacovigilance, and regulatory affairs services across 40+ countries with particular strength in oncology and rare disease.

GCP Compliant ISO 9001Phase II Clinical TrialsPhase III Clinical TrialsPhase IV / Post-Market

Iris Pharma

La Gaude, France Specialty51-200 employees

World-leading ophthalmology-specialized CRO conducting preclinical and clinical research from ocular surface to posterior segment, with 70+ ocular drugs and devices brought to market.

GLP GCP CompliantIn Vitro ScreeningPK/ADME StudiesEfficacy Studies

Lysogene

Paris, France Specialty51-200 employees

French clinical-stage gene therapy company and CRO specializing in CNS gene therapy development, providing clinical trial management for rare neurological diseases.

GCP Compliant GMPPhase I Clinical TrialsPhase II Clinical TrialsCell & Gene Therapy Manufacturing

NextPharma Technologies

Limay, France CDMO501-1000 employees

French CDMO specialising in topical, semi-solid, and liquid pharmaceutical manufacturing for clinical trial supply and commercial production.

GMP Certified FDA RegisteredFormulation DevelopmentFill-Finish ServicesPackaging & Labeling

Oncodesign Services

Dijon, France Specialty201-500 employees

European preclinical CRO in Dijon, France, specializing in oncology, inflammation, and infectious disease drug discovery including targeted radiotherapy programs.

GLP Compliant ISO 9001In Vitro ScreeningCompound ProfilingEfficacy Studies

Phinc Development

Paris, France Full Service51-200 employees

French mid-size CRO specialising in Phase I-III clinical trials, biostatistics, and regulatory affairs with offices in Paris and North Africa.

GCP CompliantPhase I Clinical TrialsPhase II Clinical TrialsPhase III Clinical Trials