Administrative Regulation No.35/2021 Organization and functioning of the Pharmaceutical Administration Bureau

Previously notified in N1MAC7 and N3MAC25
According to Administrative Regulation No. 28/2003 as revised by Administrative Regulation No. 19/2016 and Administrative Regulation No. 35/2021, the authority to issue import licenses for goods listed in group B1 of Table B is vested in the Pharmaceutical Administration Bureau.