Pharmaceutical Affairs Act Article 40-2
1. Upon the issuance of a new drug license, the central competent health authority shall publish the patent numbers or file numbers that have already been disclosed to the public as submitted by the applicant.2. Within 3 years after the issuance of a new drug license for a new molecular entity, no other pharmaceutical firm may apply for registration of the same drug by citing the application data submitted by said drug license holder without such holder’s consent.3. Starting from the next day to the expiration of the period stipulated in Paragraph 2 hereof, other pharmaceutical firms may apply for registration of drugs in accordance with this Act and relevant regulations; for those in compliance with relevant regulations, the central competent health authority may issue a drug license only after the next day to the expiration of a 5-year period after the issuance of said new drug license for the new molecular entity as stipulated in Paragraph 2 hereof.4. Paragraph 2 hereof is applicable only when an application for registration of a drug containing a new molecular entity is filed with the central competent health authority within 3 years after marketing approval is obtained for such drug in a foreign country.
中文原文 藥事法第40-2條
中央衛生主管機關於核發新藥許可證時,應公開申請人檢附之已揭露專利字號或案號。
新成分新藥許可證自核發之日起三年內,其他藥商非經許可證所有人同意,不得引據其申請資料申請查驗登記。
前項期間屆滿次日起,其他藥商得依本法及相關法規申請查驗登記,符合規定者,中央衛生主管機關於前項新成分新藥許可證核發屆滿五年之次日起,始得發給藥品許可證。
新成分新藥在外國取得上市許可後三年內,向中央衛生主管機關申請查驗登記,始得適用第二項之規定。
新成分新藥許可證自核發之日起三年內,其他藥商非經許可證所有人同意,不得引據其申請資料申請查驗登記。
前項期間屆滿次日起,其他藥商得依本法及相關法規申請查驗登記,符合規定者,中央衛生主管機關於前項新成分新藥許可證核發屆滿五年之次日起,始得發給藥品許可證。
新成分新藥在外國取得上市許可後三年內,向中央衛生主管機關申請查驗登記,始得適用第二項之規定。