CRO for Clinical Trials in France
France has a long-standing tradition of high quality clinical research and it is one of the world’s leading countries in hosting clinical trials (in the top 4 countries in Europe). By mid 2021, the clinical trial database of the United States (clinicaltrials.gov) had registered a total of 28,571 clinical studies including at least one French clinical center.
With a large estimated population of 67 million, France has a long list of top clinical sites with high enrollment rates across multiple therapeutic areas. Some of the main cities with prestigious hospitals include Paris, Lyon, and Bordeaux.
Sofpromed has capabilities to manage clinical trials in France as well as in other EU countries. We can provide a full range of CRO services for biotech and pharma companies planning clinical studies in France along with other European member states.
Our CRO services in France include:
- Regulatory affairs
- Ethics committee submissions
- Full clinical operations
- Site selection and activation
- Onsite and remote monitoring visits
- Data management
- SAS statistical programming
- Medical writing
- Clinical supply management
- Drug logistics
In French hospitals we can provide CRO services for clinical trial sponsors in the following therapeutic areas:
- Central nervous system (CNS)
- Infectious diseases
- Respiratory diseases