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Federal Act
on Medicinal Products and Medical Devices
(Therapeutic Products Act, TPA)

Art. 3 Due diligence

1Any per­son hand­ling thera­peut­ic products must take all meas­ures ne­ces­sary ac­cord­ing to the state of the art to en­sure that hu­man or an­im­al health is not en­dangered.

2 The state of the art in sci­ence and tech­no­logy must be con­sidered for com­ple­ment­ary medi­cines without in­dic­a­tions, in­clud­ing the prin­ciples of the cor­res­pond­ing ther­apy ap­proach.8

8 In­ser­ted by No I of the FA of 18 March 2016, in force since 1 Jan. 2019 (AS 2017 2745, 2018 3575; BBl 2013 1).