In addition to our own network of 1,160 laboratories, we collaborate with an extensive network of hospitals and private partners around the world to provide you with: 

– Recruitment of the patients fitting with your study’s criteria 

– Fresh and qualified sample collection 

– Kit building to ensure an efficient sample collection 

– Logistics support 

At Cerba Research, we are aware of the importance of having reliable data associated with your samples. We ensure yours are supplied with the right samples data to match your needs.

A dedicated IVD and MD clinical trials team will be beside you throughout your study, supporting you with:  

• IRB protocol writing and submissions 
• Ready-to-use IRB protocols 

• Access to 1,160 sites across Europe and Africa 
• A dedicated pathologists, regulatory affairs, CRA, biostatisticians, nurses, data managers, etc. 
• A patient identification solution to speed up the enrollment of eligible patients 
• Access to our logistical platforms 
• Analytical testing services