Contract Research Organization

Become regulatory confident

The regulatory experts at LINK Medical can guide your company through the entire regulatory pathway. Additionally we can perform a GAP analysis to assure you have the right documentation to enter the clinical phase.

They are particularly well versed in the maintenance of marketing authorization of a product, label translations and marketing compliance.

Experts in clinical methodology for all phases

LINK Medicals employees are proud to be experts in the methodology of all clinical trial phases, regardless of complexity or indication. We have specially long experience from early oncology phase I studies. Additionally, we excel in handling the complex international phase II and smaller phase III studies, all with successful delivery and high quality through our adaptive and rigid processes.

Small enough and Big enough

We are the flexible contract research organization (CRO) with solid, established processes: not only are we agile enough to be adaptive to the needs of small customers but also big enough to handle complex international studies, including smaller phase III studies.

Why not engage LINK Medical as your local preferred provider for late phase studies?

Rigid processes with quality as a strong focus

Since we are audited several times each year by international companies, both big pharma and smaller companies, we constantly receive feedback on our Standard Operating Procedures (SOPs). Consequently, we are confident that we are up to date with all the latest requirements and regulations.