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


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Art. 84 227

1 Un­less this Act provides oth­er­wise, the ad­min­is­trat­ive pro­ced­ure and rights of ap­peal are reg­u­lated by the Fed­er­al Act of 20 Decem­ber 1968228 on Ad­min­is­trat­ive Pro­ced­ure and by the Fed­er­al Ad­min­is­trat­ive Court Act of 17 June 2005229, and the Fed­er­al Su­preme Court Act of 17 June 2005230.231

1bis In ad­min­is­trat­ive pro­ceed­ings in­volving the Agency, the con­sent of as­sessors and sci­entif­ic ad­visors is re­quired be­fore their names may be dis­closed to the parties.232

2 The Agency is en­titled to ex­er­cise the rights of ap­peal un­der can­ton­al and fed­er­al law against rul­ings of the can­ton­al au­thor­it­ies and the Fed­er­al Ad­min­is­trat­ive Court in ap­plic­a­tion of this Act and its im­ple­ment­ing pro­vi­sions.233

3 It is also en­titled to ap­peal against de­cisions made by the highest can­ton­al au­thor­it­ies in ap­plic­a­tion of the Hu­man Re­search Act of 30 Septem­ber 2011234 (Art. 89 para. 2 let. a of the Fed­er­al Su­preme Court Act of 17 June 2005).235

227 Re­pealed by An­nex No 89 of the Fed­er­al Ad­min­is­trat­ive Court Act of 17 June 2005, with ef­fect from 1 Jan. 2007 (AS 2006 21971069; BBl 2001 4202).

228 SR 172.021

229 SR 173.32

230 SR 173.110

231 Amended by An­nex No 89 of the Fed­er­al Ad­min­is­trat­ive Court Act of 17 June 2005, in force since 1 Jan. 2007 (AS 2006 21971069; BBl 2001 4202).

232 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).

233 Amended by No 1 12 of the Fed­er­al As­sembly O of 20 Dec. 2006 on the Amend­ment of Le­gis­la­tion in ac­cord­ance with the pro­vi­sions of the Fed­er­al Su­preme Court Act and the Fed­er­al Ad­min­is­trat­ive Court Act, in force since 1 Jan. 2007 (AS 2006 5599; BBl 2006 7759).

234 SR 810.30

235 In­ser­ted by An­nex No 6 of the Hu­man Re­search Act of 30 Sept. 2011, in force since 1 Jan. 2014 (AS 2013 3215; BBl 20098045).

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