조문단위인쇄

PHARMACEUTICAL AFFAIRS ACT
조문단위인쇄
 Article 35 (Conditional Permission)
(1) In granting permission under Article 31 (1) and (2), the Minister of Food and Drug Safety may grant permission for the business of manufacturing drugs or items prescribed by Ordinance of the Prime Minister, on condition that the facilities referred to in Article 31 (1) be installed within a fixed period. <Amended by Act No. 8643, Oct. 17, 2007; Act No. 8852, Feb. 29, 2008; Act No. 9932, Jan. 18, 2010; Act No. 11690, Mar. 23, 2013>
(2) If a person who has obtained permission under paragraph (1) fails to be equipped with proper facilities without justifiable grounds within the period under paragraph (1), the Minister of Food and Drug Safety shall revoke such permission. <Amended by Act No. 11690, Mar. 23, 2013>