Regulations of Medicament Manufacturer Inspection Article 16
Application forms stipulated in this set of Regulations shall be determined by the central competent health authority.The inspected party shall prepare the information required for the inspection in accordance with the items stipulated in said application forms. In filling out application forms and providing accompanying information, only traditional Chinese characters and English shall be used; where text that is not in traditional Chinese or English, a traditional Chinese version or English translation must be provided.
中文原文 藥物製造業者檢查辦法第16條
本辦法之各項書表，由中央衛生主管機關定之。
受檢查業者應依書表所載事項，備齊相關資料；填寫書表及檢附之資料，限用繁體中文及英文；如非繁體中文或英文者，應另附繁體中文或英文譯本。
受檢查業者應依書表所載事項，備齊相關資料；填寫書表及檢附之資料，限用繁體中文及英文；如非繁體中文或英文者，應另附繁體中文或英文譯本。