Who are we?
European expertise driving your clinical and international success
Centaur Clinical France is a Contract Research Organization (CRO) specializing in clinical trials and clinical investigations. We are a medical devices CRO based in Europe and operating internationally. Our expert clinical team supports Biotech and Medtech companies throughout every stage of their clinical development. Our commitment: personalized support, fully compliant with regulatory requirements and tailored to the realities of each clinical project.
Our identity
Centaur Clinical France: your Europe-based CRO for medical devices
Centaur Clinical France supports pharmaceutical, medical device, IVD and health product manufacturers in the design and successful execution of their clinical studies. As a medical devices CRO in Europe, we guarantee reliable, traceable and inspection-ready data. Our team brings together clinical experts committed to compliance, scientific rigor and operational excellence.
Our integrated expertise includes:
- Design, conduct and successful completion of clinical trials and investigations
- Rigorous oversight in full compliance with ICH-GCP E6(R3), FDA requirements and ISO 14155
- A structured quality system certified ISO 13485 (ISO 9001 in progress)
- Tailored support for each clinical project
- Integrated clinical, regulatory and operational expertise
- A multidisciplinary team: clinical experts, quality and regulatory specialists, medical writers, vigilance experts and data specialists
- Synergy with our Algeria CRO subsidiary specialized in clinical trials and bioequivalence studies
Data & Certifications
Our commitment
Controlled deadlines
At Centaur Clinical, customer satisfaction is a priority. Our agile and responsive team does everything possible to respond to your requests quickly and efficiently. Our experts are available, accessible, and attentive throughout the study. Whatever your issue, they will advise you and offer you the right solutions.
We guarantee:
- personalized support tailored to each clinical project;
- a dynamic team that is attentive to your needs and dedicated to the success of your clinical studies;
- optimized completion times.
A controlled budget
Each quote is prepared based on an in-depth discussion with the client in order to fully understand their needs and expectations. Services are described transparently, item by item, for complete clarity. This approach allows us to offer a tailored and controlled budget with no surprises.
In addition, our in-house clinical, regulatory, and operational expertise enables us to offer competitive rates in the clinical trial market.
Our values
Scientific excellence, compliance and certification
Our actions are guided by a commitment to rigor, transparency, and compliance.
Our studies are built on an approach of operational excellence that ensures data quality and patient safety.
Rigor and compliance
Our activities are guided by high standards of scientific rigor, transparency and regulatory compliance.
We apply all relevant international standards:
- ICH-GCP E6(R3)
- European regulations
- FDA requirements
- ISO 14155
This strict framework ensures safe, compliant and high-quality clinical trials.
Operational excellence
Our clinical studies follow a continuous improvement approach:
- Process optimization
- Systematic quality control
- Scientific rigor at every stage of the clinical project
Human commitment and close collaboration
We work directly with manufacturers, offering:
- A dedicated point of contact
- Consistent availability
- Personalized guidance from study design to completion
Data quality and traceability
Our robust internal SOPs ensure:
- Full data traceability
- Consistent, inspection-ready datasets
- Full GDPR compliance for personal data protection
Multidomain expertise throughout the full clinical and regulatory lifecycle
Our CRO supports you across all phases of clinical development through integrated expertise in:
- Pharmaceutical clinical trials
- Medical device and IVD clinical investigations (CE marking and PMCF)
- Data management
- Regulatory affairs and quality
- Medical writing
- Pharmacovigilance and materiovigilance
- Clinical technologies
Rigor and compliance
Our activities are guided by high standards of scientific rigor, transparency and regulatory compliance.
We apply all relevant international standards:
- ICH-GCP E6(R3)
- European regulations
- FDA requirements
- ISO 14155
This strict framework ensures safe, compliant and high-quality clinical trials.
Data quality and traceability
Our robust internal SOPs ensure:
- Full data traceability
- Consistent, inspection-ready datasets
- Full GDPR compliance for personal data protection
Operational excellence
Our clinical studies follow a continuous improvement approach:
- Process optimization
- Systematic quality control
- Scientific rigor at every stage of the clinical project
Human commitment and close collaboration
We work directly with manufacturers, offering:
- A dedicated point of contact
- Consistent availability
- Personalized guidance from study design to completion
Multidomain expertise throughout the full clinical and regulatory lifecycle
Our CRO supports you across all phases of clinical development through integrated expertise in:
- Pharmaceutical clinical trials
- Medical device and IVD clinical investigations (CE marking and PMCF)
- Data management
- Regulatory affairs and quality
- Medical writing
- Pharmacovigilance and materiovigilance
- Clinical technologies
Contact
Quality and certifications
Centaur Clinical CRO France is ISO 13485 certified and currently engaged in the ISO 9001 certification process to ensure a high-performing, structured and efficient quality management system.
Need information about our certifications?
Social responsibility
CSR at the heart of our corporate strategy
Our commitments
Human values and sustainable development are central to our corporate identity. Ethics, responsibility and positive impact guide all our actions.
Our CSR framework
Our CSR approach is based on the international standard ISO 26000, built around seven pillars:
- Organizational governance
- Labour relations and working conditions
- Fair business practices
- Community involvement and local development
- Human rights
- Environmental responsibility
- Consumer issues
Our approach
We joined the CEDRE PACA 2021–2023 program to strengthen and structure our CSR strategy.
This initiative, led by the SUD Region (France), supports companies in ecological transition, circular economy development and responsible business practices.
Our impact
We contribute to a sustainable, responsible development model aligned with current societal, environmental and economic expectations.
Our commitments
Human values and sustainable development are central to our corporate identity. Ethics, responsibility and positive impact guide all our actions.
Our approach
We joined the CEDRE PACA 2021–2023 program to strengthen and structure our CSR strategy.
This initiative, led by the SUD Region (France), supports companies in ecological transition, circular economy development and responsible business practices.
Our CSR framework
Our CSR approach is based on the international standard ISO 26000, built around seven pillars:
- Organizational governance
- Labour relations and working conditions
- Fair business practices
- Community involvement and local development
- Human rights
- Environmental responsibility
- Consumer issues
Our impact
We contribute to a sustainable, responsible development model aligned with current societal, environmental and economic expectations.
Meet us
Let’s talk about your project
A project manager or regulatory expert will get back to you quickly to assess your needs and propose a clinical pathway tailored to your market objectives.
