Eurofins, an eminence in clinical trials
For over three decades, Eurofins Optimed has orchestrated and executed clinical trials on behalf of sponsors from the Pharma, Biotech, Medtech and Foodtech industries in order to help them develop life-saving and life-improving products.
Specialized in Early Clinical Development
Since we focus on Early Clinical Development, we are cognizant of the distinctive importance and the urgency of First-in-Human (FIH) and Early Phase clinical trials.
We understand how to meet your every specific technical and operational requirements so that you can make the best science and data-driven go/no-go decisions in a timely manner.
Quality transparency and accountability are the cornerstone of our success, and of yours.
Do not make concessions when it comes to the integrity of your clinical trial. Rigorous regulatory scrutiny is necessary and benefits everyone: patients, sponsors, regulators and clinical trial service providers.
One-stop shop or pick and mix services.
Whether you are the Head of Clinical Operations of a big Pharmaceutical or Medical Device multinational company, or the founder of a small biotechnology start-up, your needs for external support may vary significantly.
Because your project is unique and requires an individual approach, we provide a comprehensive range of bespoke and adaptable solutions on a stand-alone or full-service package basis.
An all In-house approach
By virtue of Eurofins’ worldwide network of laboratories and dedicated GxP Pharma sites, underpinned by its robust QA programme, we are in an unrivalled position to undertake internally the entire spectrum of activities required to direct and support clinical trials. This allows us to optimize the time and cost of your clinical development projects.
Full-Service Clinical Research Organization
- Clinical Trial Protocol
- Regulatory Affairs
- Medical Writing
- Global trial and site management (Project Management, Monitoring and Vigilance)
- Subject Recruitment Services
- Biometry Services
- Biology Services
- GMP product Manufacturing and Development services
Early Clinical Trials Unit (CTU)
Standard First’-into-human (FIH)
- Early QT assessment)
- Bioavailability/ bioequivalence
- Drug/Drug interaction
- Food effect
- Dose proportionality
- Muscle biopsy
- Micro dosing
- Glucose Clamp
- Sleep Evaluation