(iii)
the conditions under which the clinical trial is to be conducted, including the expected duration of the subject's participation in the clinical trial; and
← art_29__para_2__point_a__point_ii__text_1 · All articles · art_29__para_2__point_a__point_iii__text_1 →
Source: EUR-Lex (Cellar) · retrieved 2026-11-06 · Text as adopted (Official Journal); later amendments are not incorporated in this text.