Optimed
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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.
Commitment to Quality and Compliance
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. Quality transparency and accountability are the cornerstone of our success, and of yours.
Eurofins Optimed, your end-to-end GxP clinical trial solutions
Full-Service Clinical CRO
Clinical Trials Unit (CTU)
A-to-Z, from protocol design through to study report, Eurofins Optimed is your fully customizable one stop-shop spanning the entire ecosystem of clinical research solutions.
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Clinical trial protocol
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Regulatory affairs
- Global trial and site management
- Clinical project management, monitoring and vigilance
- Subject recruitment
- Biometry (Data management, biostatistics and study report)
- Medical writing
- Clinical biology and laboratory operations
- API manufacturing, development and distribution (CDMO)
Dedicated to early clinical development in healthy volunteers and ambulatory patients.
- Early QT assessment
- Bioavailability/ bioequivalence
- Biosimilars
- Drug/Drug interaction
- Food effect
- Pharmacodynamics
- Pharmacokinetics
- Dose proportionality
- First-in-Human (SAD, MAD)
- Tobacco products
- Vaccines
- Muscle biopsy
- Micro-dosing
- Glucose clamp
- Sleep evaluation
