CEBIS has access to more than 300 research sites in North America, Europe and India.
Based on years of experience and taking into consideration the aspects of the clinical trials protocols, we perform the feasibilities and the site selection to fit the best way with your plans.
Quick start-up process
Short negotiation timelines for contracts
Hight quality of medical data
Quick answer to the queries
Focus on data base lock
Applying rule of 5:5:5
5 days to complete EDC, 5 days to answer to the queries, 5 days to close the sites specific action items
We’d love to hear more about your needs
Even if you are still in the planning stages of your project, you are more than welcome to submit a request to us. We can assist you with a quotation or create a proposal for you based on the minimum information you can provide.