Regulations Governing Management of Infectious Biological Materials Article 31

The competent authority may, for the needs of disease prevention and control, order high-containment laboratories, controlled premises, or laboratories and storage facilities that use and store pathogens in Risk Groups 2-4 or biotoxins, to provide relevant documents and information, and may conduct supervision and inspection thereof.When deficiencies are found in the supervision or inspection conducted pursuant to the preceding paragraph, the competent authority shall order the entity to take corrective actions within a given period of time; if the entity fails to comply accordingly, the competent authority may order the entity to discontinue the possession, storage, use, or disposition of relevant infectious biological materials, or suspend the operations of the aforementioned premises in part or in whole.Entities and their personnel may not evade, interfere with, or refuse the supervision, inspection, and actions taken by competent authorities under the preceding two paragraphs.
中文原文 感染性生物材料管理辦法第31條
主管機關得對高防護實驗室、管制作業場所或實驗室、保存場所使用、保存第二級至第四級危險群病原體或生物毒素者,得因防疫需要令其提供相關文件、資料,並進行督導、查核。
經前項督導、查核發現有缺失者,主管機關應通知其限期改善;屆期未改善者,主管機關得要求其停止持有、保存、使用或處分相關感染性生物材料或暫停前項場所之全部或一部運作。
前二項主管機關之督導、查核及處置,設置單位及其人員不得規避、妨礙或拒絕。

English translation for reference only; the Chinese text prevails. Not legal advice.