Clinical research CRO services

CRO services for clinical research

We provide full-service clinical research support for pharmaceuticals, ATMPs, biologics, medical devices, in vitro diagnostic (IVD) medical devices, and combination products. With dedicated teams in the Nordics, Germany, and Poland, our contract research organization (CRO) supports clients across pharma, biotech, medtech, and academia in the design and execution of clinical studies.

In addition to our in-house capabilities, we leverage a robust network of trusted partners across Europe. By partnering with us, you can be confident that we will provide you with the expert support that you need to succeed. In addition to our dedication and expertise, our relationship-focused approach makes all the difference – it’s vital for the project’s success and is truly valued by our customers.

We provide custom and flexible solutions that meet your unique needs – from designing and carrying out clinical studies to developing an entire clinical program. 

Our services cover:

• Feasibility assessment and site evaluation
• Clinical project management
• Site start-up, site management and clinical monitoring
• Regulatory submissions
• Medical writing 
• Data management and biostatistics
• Pharmacovigilance and vigilance
• Outsourcing services for when you need extra resources/interim solutions.
• Quality and regulatory services