REGULATIONS FOR APPLICATION OF HEALTH FOOD PERMIT Article 23
The documentary evidence in Subparagraph 9 of Paragraph 1 of Article 2 shall include the documents of the control for the manufacturing process and quality control, engineering diagrams of quality control and other documents and information verifying compliance with good manufacturing practices.The documents and information in the preceding paragraph may be substituted with officially certificate documents verifying compliance with the respective good manufacturing practices from the country of origin for imported products; the certificate documents within effective period to be verified compliance with the Pharmaceutical Good Manufacturing Practice Regulations by the central competent authority shall be provided for domestic products manufactured by the pharmaceutical companies.
中文原文 健康食品申請許可辦法第23條
第二條第一項第九款佐證資料，應包括製程管制文件、品質管制文件、品管工程圖及其他證明符合生產國良好作業規範規定之文件、資料。
產品為輸入者，前項文件、資料得以原產國官方出具符合該國良好作業規範之證明文件代之；為國內生產且由藥廠兼製者，應提出經中央主管機關查核符合藥物優良製造準則且於有效日期內之證明文件。
產品為輸入者，前項文件、資料得以原產國官方出具符合該國良好作業規範之證明文件代之；為國內生產且由藥廠兼製者，應提出經中央主管機關查核符合藥物優良製造準則且於有效日期內之證明文件。