From phase I to phase III

To support you in:

• Conception
• Starting from a synopsis we can create:

>Protocol >electronic or paper CRF

• The request for authorisation towards the agencies and the Ethics Committees
In France
In Europe,
In the U.S.A.

• The installation, the investigators’ meeting.
• Monitoring
• Management of cost overruns, invoices
• Pharmacy
• Follow-up
• Closures
• Medical writing