Full clinical CRO and CDMO package
Eurofins CDMO network of companies and Eurofins Optimed SAS,
your End-to-End Clinical Development Partners
With a joint end-to-end clinical development offer, Eurofins CDMO network of companies and Eurofins Optimed SAS help you bring Investigational Medicinal Product (IMP) to market authorization, from patient recruitment to manufacturing scale-up.
Eurofins CDMO network of companies can support you on preclinical and clinical stages on:
- Preformulation, formulation development
- Drug product manufacturing
- Clinical trial supply and logistics
- CMC-RA support
Eurofins Optimed SAS (clinical-stage full service CRO) can help you with:
- Protocol development and study design
- Regulatory analysis, submission and interaction with the authorities
- Site and trial monitoring and management
- Bio-analysis (DMPK, Biomarkers, specialized biology)
- Biometry (Data Management, Biostatistics and writing of CSR
For over three decades, we have successfully executed clinical trials on behalf of sponsors from the Pharma, Biotech, Medtech.
