Ordinance
on Human Research with the Exception of Clinical Trials
(Human Research Ordinance, HRO)


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Art. 29 Informed consent for further use of biological material and genetic personal data in coded form for research purposes

1 The per­sons con­cerned must re­ceive writ­ten or or­al in­form­a­tion on:

a.
the pro­posed fur­ther use of the coded bio­lo­gic­al ma­ter­i­al and coded ge­net­ic per­son­al data for re­search pur­poses;
b.
their right to with­hold or to re­voke their con­sent at any time without giv­ing reas­ons;
c.
meas­ures to pro­tect the bio­lo­gic­al ma­ter­i­al and per­son­al data, and in par­tic­u­lar man­age­ment of the key;
d.
the pos­sib­il­ity of the bio­lo­gic­al ma­ter­i­al and the ge­net­ic per­son­al data be­ing passed on to third parties for re­search pur­poses.

2 Con­sent must be giv­en in writ­ing; the ex­cep­tions are gov­erned by Art­icle 9 mu­tatis mutandis.

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