Services

We offer expert services for your entire product development journey. Flexible standalone help, or full-service support for a complete clinical study. You choose.

Our services

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

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

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

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

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Medical experts with industry experience.

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

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

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

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

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

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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?

590 +

clinical trials

150 +

employees

20 +

therapeutic areas

6

countries

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