Pharmacovigilance

Pharmacovigilance is the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other medicine-related problem.

Pharmacovigilance system

The European Medicines Agency (EMA) coordinates the European Union (EU) pharmacovigilance system and operates services and processes to support pharmacovigilance in the EU. It is essential that the safety of all medicines is monitored throughout their use in healthcare practice. EU law requires each marketing authorisation holder, national competent authority and EMA to operate a pharmacovigilance system. The situation is similar in Switzerland, which is not in the EU but has equally strict requirements policed by its agency, SwissMedic. We know and worked with the right consultants whom have extensive experience in pharmacovigilance.

Let us commercialise your pharmaceuticals.

We know these local markets, and this gives you the best opportunity for commercialising your specialized (niche) pharmaceuticals. 1 single point of contact gives you the possibility to have your products available to 200 million Europeans in 28 countries. For all 28 countries or a selection of these countries.

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