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


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Art. 7 Manufacturing standards

1 The man­u­fac­ture of medi­cin­al products and phar­ma­ceut­ic­al ex­cipi­ents whose man­u­fac­ture re­quires a li­cence must con­form to the re­cog­nised rules of good man­u­fac­tur­ing prac­tice.29

2 The Fed­er­al Coun­cil shall spe­cify the re­cog­nised rules of good man­u­fac­tur­ing prac­tice. In do­ing so, it shall take ac­count of in­ter­na­tion­ally re­cog­nised guidelines and stand­ards.

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

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