Which evidence is required for Market Access in Germany?

In Germany, evidence is one of the key factors for the successful Market Access of medical devices. Planning and realization of clinical and economic studies but even the preparation of already existing evidence can be effective to achieve Sales and Market Access goals.

Healthcare Heads has a broad experience in the preparation of existing evidence for defined purposes as well as the preparation and design of new studies according to the requirements.

We might help you to decide which type of evidence is required to achieve your goals.

The type of evidence required depends on the target group and several other parameters, e.g. the product itself, the indication, the patients, the alternative therapy, the price etc.

We are specialized in navigating you through the different requirements on evidence - please do not hesitate to contact us for further information.


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Phone: +49 431 800 147 0