Your end-to-end clinical development partners
With a joint end-to-end clinical development offer, Eurofins CDMO and Eurofins Optimed help you bring Investigational Medicinal Product (IMP) to market authorization, from patient recruitment to manufacturing scale-up.
Eurofins CDMO expertise
Eurofins CDMO can support you on preclinical & clinical stages on:
- Preformulation, formulation development
- Drug product manufacturing
- Clinical trial supply and logistics
- CMC-RA support
Eurofins Optimed (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
A new clinical study to manage?