Regulations for Reporting Serious Adverse Reactions of Medicaments Article 12
The central competent health authority may delegate the receipt, request for correction, or provision of relevant documents and data specified in the Regulations to its subordinate agencies or entrust relevant agencies (institutions), juridical persons, or groups to handle such matters.
中文原文 嚴重藥物不良反應通報辦法第12條
本辦法所定通報之受理、要求補正或提供相關文件、資料，中央衛生主管機關得委任所屬機關或委託相關機關（構）、法人或團體辦理。