Regulations for Registration of Medicinal Products Article 5
The term “authorization letter” mentioned in this Chapter refers to the documents issued by the foreign manufacturer, headquarters or the license holder of an imported drug to authorize the application of drug registration.The above-mentioned authorization letter is effective for one year from the issuance date. The authorization letter should include the names and addresses of the manufacturer and the agent, as well as drug name, dosage form and contents. The information should be consistent with those stated in the application form. If the authorization letter is in neither Chinese nor English, a Chinese or English translation should be provided additionally.If the original license holder has a branch office in Taiwan, the authorization letter can be issued by either the manufacturer’s headquarters or the head office in Asia.
中文原文 藥品查驗登記審查準則第5條
本章所稱委託書，係指輸入藥品之國外製造廠或其總公司、或國外許可證持有者所出具之授權登記證明文件。
前項委託書限出具日起一年內有效，且內容應載明製造廠及代理商之名稱、地址，與藥品名稱、劑型及含量，並其記載應與申請書相符。
如委託書非中文或英文者，應附中文或英文譯本。
如持有出產國藥品製造許可證之製造廠於中華民國境內（以下簡稱國內）設有分公司者，其委託書得由該製造廠之總公司或設於亞洲之總部出具。
前項委託書限出具日起一年內有效，且內容應載明製造廠及代理商之名稱、地址，與藥品名稱、劑型及含量，並其記載應與申請書相符。
如委託書非中文或英文者，應附中文或英文譯本。
如持有出產國藥品製造許可證之製造廠於中華民國境內（以下簡稱國內）設有分公司者，其委託書得由該製造廠之總公司或設於亞洲之總部出具。