Services

Deep knowledge of the local regulations in the Nordics and extensive experience engaging with the national Competent Authorities and notified bodies.

We always stay up to date with national legislation, marketing and advertising guidelines, and local ethical codes.

CRAs in the Nordic, UK and Germany but also covering Switzerland and Austria.

A highly skilled Clinical Project Manager (CPM) is a pre-requisite for a successful clinical study.

Medical experts with industry experience.

Highly scientific team with thorough knowledge of GCP ICH guidelines, and ISO standards can prepare your protocol, investigational plan or study report as example.

Technology driven Data Managers, specialists in eCRF set-up, data collection, validation, and data base locking.

Senior team offering a wide range of statistical services, guidance and expertise.

Dedicated partner in clinical safety and post marketing phv services; from inception to success.

Develop strategies that optimize your product’s lifecycle in today’s challenging and shifting healthcare landscape and competitive market.

Highly qualified and competent QA unit covering all GxPs.
From non-clinical and clinical trials, manufacturing, distribution, and safety.
Need help with developing a QMS?