Com­pa­ny

The in.vent is com­mit­ted to the high­est eth­i­cal stan­dards and always observes the prin­ci­ples of the Dec­la­ra­tions of Helsin­ki and Taipei as defined by the World Med­ical Asso­ci­a­tion in all projects. Our med­ical coop­er­a­tion part­ners are con­trac­tu­al­ly com­mit­ted to com­ply­ing with and com­ply­ing with these stan­dards. Our projects are eval­u­at­ed and eval­u­at­ed by com­pe­tent inde­pen­dent ethics com­mit­tees and, if nec­es­sary, by the com­pe­tent fed­er­al author­i­ty. In doing so, we take into account: the notes of the Fed­er­al Med­ical Asso­ci­a­tion and the “Work­ing Group of Med­ical Ethics Com­mit­tees in the Fed­er­al Repub­lic of Ger­many e.V.”, the Europe-wide Gen­er­al Data Pro­tec­tion Reg­u­la­tion, ISO 20916 (in-vit­ro diag­nos­tic med­ical devices — Clin­i­cal per­for­mance stud­ies using spec­i­mens from human sub­jects — Good study prac­tice) and ISO 20387 (Biotech­nol­o­gy — Biobank­ing — Gen­er­al require­ments for biobank­ing) and are thus able to ful­ly com­ply with the eth­i­cal prin­ci­ples required by IVDR 2017/746.