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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). |