Ionizing Radiation Protection Act Article 30

Production Permits and RequirementsParagraph 30.1One shall not produce radioactive material, construct its production facilities, or manufacture equipment capable of producing ionizing radiation until after the Competent Authority reviews the application and issues a permit.Paragraph 30.2The operation of facilities producing radioactive material shall be conducted by qualified operation personnel.The qualification of operation personnel, and the issuance, period of validity, renewal, replacement, or termination of certificates or licenses, as well as other regulations to abide by shall be laid down by the Competent Authority.Paragraph 30.3Production or manufacturing in Paragraph 30.1 shall be registered with the Competent Authority within fifteen (15) days after the work starts. The records on production or manufacturing, inventory and sales shall be submitted to the Competent Authority on a regular basis. The Competent Authority may dispatch officers to perform on-site inspection at any time.Paragraph 30.4If the production of radioactive material or manufacturing of equipment capable of producing ionizing radiation in Paragraph 30.1 is for medical purposes, it shall also comply with central government health regulations.
中文原文 游離輻射防護法第30條
放射性物質之生產與其設施之建造及可發生游離輻射設備之製造,非經向主管機關申請審查,發給許可證,不得為之。
放射性物質生產設施之運轉,應由合格之運轉人員負責操作;其資格、證書或執照之核發、有效期限、換發、補發、廢止及其他應遵行事項之辦法,由主管機關定之。
第一項生產或製造,應於開始之日起十五日內,報請主管機關備查;其生產紀錄或製造紀錄與庫存及銷售紀錄,應定期報送主管機關;主管機關得隨時派員檢查之。
第一項放射性物質之生產或可發生游離輻射設備之製造,屬於醫療用途者,並應符合中央衛生法規之規定。

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