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My market access expertise includes the reimbursement and pricing of pharmaceuticals and medical devices in the stationary and outpatient service areas of the statutory health insurance (GKV), including practice assessment procedures before the Federal Joint Committee (G-BA) and negotiations with statutory health insurance companies and the GKV-Spitzenverband.

The regulatory consulting practice particularly encompasses placing pharmaceuticals and medical devices on the market (conformity assessment procedures, authorisation, distribution, GDP, contracts between different parts of the supply chain), wholesale authorisations, compassionate use and individual imports, clinical trials and good manufacturing practice. I have special expertise in the fields of unfair competition, particularly the laws on advertising pharmaceutical products and the cooperation between the industry, experts and patient organisations.

I am also regularly representing companies before the authorities and in court.

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