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Fee-Charging Standards for Lot Release, Reference Materials, and Testing of Foods, Drugs and Cosmetics
1.中華民國一百年十二月三十日行政院衛生署署授食字第 1001904420 號 令訂定發布全文 4 條；除另定施行日期者外，自發布日施行 2.中華民國一百零二年十月二日衛生福利部部授食字第 1021950561 號令 修正發布第 1 條條文 3.中華民國一百零四年四月九日衛生福利部部授食字第 1041900335 號令 修正發布全文 4 條；除附表自一百零四年七月一日施行外，其餘條文 自發布日施行 4.中華民國一百零五年八月二十九日衛生福利部部授食字第 1051901465 號令修正發布第 2 條附表 5.中華民國一百零八年六月二十一日衛生福利部衛授食字第 1081900724 號令修正發布第 2 條附表 6.中華民國一百十年三月二十六日衛生福利部衛授食字第 1101900513 號 令修正發布第 1 條條文及第 2 條條文之附表 7.中華民國一百十三年七月十一日衛生福利部衛授食字第 1131901181 號 令修正發布全文 4 條；並自發布日施行
資料來源：全國法規資料庫（ChOrder.json，版本 2026/7/24 上午 12:00:00）・政府資料開放授權
These standards are established pursuant to Article 58 of the Act Governing Food Safety and Sanitation, Paragraph 2 of Article 104-2 of the Pharmaceutical Affairs Act, Paragraph 2 of Article 76 of the Medical Devices Act, Article 30 of the Cosmetic Hygiene and Safety Act, and Article 10 of the Charges and Fees Act.
Contents of the standards are laid down in the Appendix.
On grounds for humane or relief purposes, biological preparations in the D numbering section of the Appendix that donated by international organizations, countries or pharmaceutical corporations can be exempted from all fees upon approval by the central competent authorities.
These standards shall be implemented as of its being promulgated.