The Plasma Derivatives Act Article 11
Plasma derivative manufacturers and importers shall periodically report their estimated and actual manufactured or imported quantity of plasma derivatives to the central competent authority for further reference.
中文原文 血液製劑條例第11條
血液製劑製造、輸入業者，應定期將其預估及實際製造或輸入之血液製劑數量，報請中央主管機關備查。