Prevention of Rare Diseases and Orphan Drug Act Article 13

Rare disease patients or their legal guardians may apply to the central competent authority by submitting an application form, together with certificates, care plans, and relevant documents issued by a medical care or research institution specified in Article 10; after review and approval by the Review Committee, the central competent authority may provide subsidies for patients to travel overseas and participate in international medical cooperation projects.When the medical cooperation project referred to in the preceding Paragraph involves laboratory testing, the application for subsidies may be made by a medical care or research institution specified in Article 10.The central competent authority shall stipulate the application procedures, required documents, and other matters to be complied with for subsidies mentioned in the preceding two Paragraphs.
中文原文 罕見疾病防治及藥物法第13條
罕見疾病病人或其法定代理人得備具申請書、第十條規定之醫療或研究機構出具之證明書、診療計畫書及相關證明文件,向中央主管機關提出申請,經審議會審議通過後,中央主管機關得提供補助至國外進行國際醫療合作。
前項醫療合作為代行檢驗項目者,得由第十條規定之醫療或研究機構申請補助。
前二項補助之申請程序、應備之書證資料及其他應遵行事項之辦法,由中央主管機關定之。

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