Partners are all actors who actively contribute to the work of the Partnership. The Partnership is open to a wide range of European and national associations, governmental and non-governmental organizations and their representatives, private sector, legal entities and individual experts, and other stakeholders. Partners are identified according to the needs of the Patient Access Partnership and its activities.
Unless confirmed in written form, the Partners are in no way responsible/obliged to comply with any official correspondence, document, report from a working group, and public statements by legal representatives of the Patient Access Partnership. The Partnership is not responsible for any actions, statements etc. of its individual partners.