Patent Act Article 91

Compulsory licensing of pharmaceuticals: export and remunerationPharmaceutical product(s) produced under compulsory licensing pursuant to the preceding Article shall be exported to the importing country entirely, and the quantity of the product authorized to be produced shall not be more than the quantity required by the importing country in its notice sent to the Council for Trade-related Aspects of Intellectual Property Rights or the foreign affairs authorities of the ROC.Pharmaceutical product(s) produced under compulsory licensing granted pursuant to the preceding Article and the external packaging thereof shall be marked with the license basis specified by the Specific Patent Agency; the packaging, coloring or shaping of the pharmaceutical product(s) produced under compulsory licensing shall be sufficiently distinguishable from pharmaceutical product(s) produced by the patentee or his/her licensee(s).The licensee of a compulsory license shall pay appropriate remuneration to the patentee. The amount of remuneration shall be decided by the Specific Patent Agency, taking into account the economic value of the patent of the required pharmaceutical product(s) to the importing country with reference to the human development index issued by the United Nations.Before exporting the pharmaceutical product(s) produced under a compulsory license, the licensee shall post on a website the quantities, name(s) and destination(s) of such pharmaceutical product(s), as well as distinctive features thereof.Inspection and registration of the pharmaceutical product(s) produced and exported under compulsory licensing pursuant to the preceding Article shall not be bound by Paragraph 2, Article 40-2 of the Pharmaceutical Affairs Act.
中文原文 專利法第91條
依前條規定強制授權製造之醫藥品應全部輸往進口國,且授權製造之數量不得超過進口國通知與貿易有關之智慧財產權理事會或中華民國外交機關所需醫藥品之數量。
依前條規定強制授權製造之醫藥品,應於其外包裝依專利專責機關指定之內容標示其授權依據;其包裝及顏色或形狀,應與專利權人或其被授權人所製造之醫藥品足以區別。
強制授權之被授權人應支付專利權人適當之補償金;補償金之數額,由專利專責機關就與所需醫藥品相關之醫藥品專利權於進口國之經濟價值,並參考聯合國所發布之人力發展指標核定之。
強制授權被授權人於出口該醫藥品前,應於網站公開該醫藥品之數量、名稱、目的地及可資區別之特徵。
依前條規定強制授權製造出口之醫藥品,其查驗登記,不受藥事法第四十條之二第二項規定之限制。

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