End-to-end clinical trial services tailored to your needs

Your expert partner for clinical trial excellence in the Nordics and Baltics 

With deep local expertise and a flexible, service-driven approach, we help you plan and conduct trials that reflect the real needs of your study with tailored support that fits your goals, timelines and regulatory requirements.

We are recognised for our commitment to quality, regulatory compliance and responsive service. Our services cover the end-to-end clinical trial support, including quality assurance, monitoring, and comprehensive coordination. We manage the entire logistics chain for investigational medicinal products - from the receipt of incoming goods to final product disposal.  And if you are designing patient-centric trials, we’re here to co-create strategies that deliver real impact.

High-quality monitoring and coordination services by experienced professionals 

• Clinical trial project management
• Site selection and feasibility assessments
• Local support with applications to Regulatory Authorities (Part II)
• Participant recruitment and retention
• Clinical trial monitoring from site initiation to close-out
• Ensuring compliance with local and international regulations
• Medical device studies
• Training and consulting services related to clinical trials 

Clinical Trial Logistics services for your study medicines (Finland and Sweden) 

• Import services
• Storage, delivery, return and disposal
• Tailored documentation and reporting solutions
• Close co-operation with clients and study sites
• Handling of named patient program products
• Labelling of study medicines in GMP-compliant secondary packaging facilities