About us

Highly experienced regulatory experts will provide you and your contracted local CROs with competent, quick and cost-efficient legal representation services within the European Union and Switzerland.

The EU Directive for Clinical Trials requests for a pharmaceutical company intending to perform clinical trials in the EU to either be established in the EU or represented by a so called “legal representative”. Likewise, the Swiss Ordinance on Clinical Trials asks for a non-Swiss pharmaceutical or medical device company to appoint a Swiss representative for clinical trials conducted in Switzerland. Additionally, national legislation of some EU member states demands that for clinical investigations with medical devices there must either be a sponsor in the EU or the sponsor must assign an EU representative.