Legal Regulations

Taiwan customs law database. Search import/export, customs, trade, and food safety rules. 34812 records.

Showing 20 / 34812 legal regulations

• Regulations for the Assessment and Approval Process of Hazardous Medical Device｜Regulations for the Assessment and Approval Process of Hazardous Medical Device - Article 2

  The so-called medical device which may cause hazard (hereinafter referred to as hazardous medical device) in the Act means that its use shall be stric...

  Ministry of Health and Welfare
• 身心障礙者鑑定作業辦法｜身心障礙者鑑定作業辦法 - Article 2

  本辦法所稱衛生主管機關：在中央為衛生福利部；在直轄市為直轄市政府；在縣（市）為縣（市）政府。

  Ministry of Health and Welfare
• Pharmaceutical Affairs Act Enforcement Rules｜Pharmaceutical Affairs Act Enforcement Rules - Article 2

  Terms used in Article 7 of the Act are defined as follows: 1. New composition: a newly invented composition that can be used for pharmaceutical purpo...

  Ministry of Health and Welfare
• Regulations on Management of Medicament Samples and Gifts｜Regulations on Management of Medicament Samples and Gifts - Article 2

  For a medicament that meets one of the requirements of the following subparagraphs, an application may be made to have it declared a medicament sample...

  Ministry of Health and Welfare
• Regulations of Medicament Manufacturer Inspection｜Regulations of Medicament Manufacturer Inspection - Article 2

  Medicament manufacturers that shall be inspected in accordance with this set of regulations are as follows: (1) Firms in the manufacturing, processin...

  Ministry of Health and Welfare
• Enforcement Rules for the Controlled Drugs Act｜Enforcement Rules for the Controlled Drugs Act - Article 2

  Institutions or business with registration licenses, whose medical or educational researchers are making application to dispense controlled drugs in a...

  Ministry of Health and Welfare
• Enforcement Rules of Cosmetic Hygiene and Safety Act｜Enforcement Rules of Cosmetic Hygiene and Safety Act - Article 2

  Cosmetics product notification and product information file stipulated under Paragraph 1 of Article 4 and the product recall as set forth under Paragr...

  Ministry of Health and Welfare
• 罕見疾病藥物供應製造及研究發展獎勵辦法｜罕見疾病藥物供應製造及研究發展獎勵辦法 - Article 2

  具有下列情形之一者，得依本辦法申請獎勵： 一、引進罕見疾病藥物、或將罕見疾病藥物列入處方集、或專案申請罕見疾病藥物，對罕見疾病藥物之供應，著有貢獻者。...

  Ministry of Health and Welfare
• 罕見疾病藥物專案申請辦法｜罕見疾病藥物專案申請辦法 - Article 2

  罕見疾病藥物未經查驗登記，或持有許可證者無法供應，或該藥物售價經中央主管機關認定顯不合理時，其製造或輸入得由政府機關、醫療機構、罕見疾病病人與家屬及相...

  Ministry of Health and Welfare
• 罕見疾病藥物查驗登記審查準則｜罕見疾病藥物查驗登記審查準則 - Article 2

  申請罕見疾病藥物查驗登記之藥商，應填具申請書，連同審查費及下列文件，送請中央主管機關核辦： 一、標籤、仿單及證照。 二、相關療效、品質及安全性資料。...

  Ministry of Health and Welfare
• 藥品查驗登記審查準則─人用血漿製劑之查驗登記｜藥品查驗登記審查準則─人用血漿製劑之查驗登記 - Article 2

  人用血漿製劑應檢附之資料： 一、血漿原料來源之管制： 二、血漿原料規格： 三、產品製造及純化過程 四、病毒去活化/去除確效資料 五、血漿製劑藥品技術性...

  Ministry of Health and Welfare
• 藥品查驗登記審查準則－生物性體外診斷試劑之查驗登記｜藥品查驗登記審查準則－生物性體外診斷試劑之查驗登記 - Article 2

  生物性體外診斷試劑應檢附之資料： 一 原料與半製品之規格與分析方法： 二 產品製造及純化過程： 三 產品之規格與技術性資料： 四 製程管制或批次製...

  Ministry of Health and Welfare
• 藥品查驗登記審查準則－疫苗類藥品之查驗登記｜藥品查驗登記審查準則－疫苗類藥品之查驗登記 - Article 2

  疫苗類藥品應檢附之資料： 一 疫苗類原料藥的定義及化學、製造與管制的要求 二 疫苗類原料藥之製造方法 三 疫苗類原料藥之製程管制資料 四 疫苗類原料藥...

  Ministry of Health and Welfare
• Enforcement Rules of the Act Governing Food Safety and Sanitation｜Enforcement Rules of the Act Governing Food Safety and Sanitation - Article 2

  The term “infant and follow-up formula” prescribed in Subparagraph 2 of Article 3 of this Act shall include infant formula, follow-up infant formula a...

  Ministry of Health and Welfare
• Enforcement Rules of Health Food Control Act｜Enforcement Rules of Health Food Control Act - Article 2

  For the purposes of paragraph 2 of Article 6 of the Act, the term "specific nutrient" shall denote substance with definite health care effects and so...

  Ministry of Health and Welfare
• Regulations Governing the Management of the Review, Registration and Issuance of Permit Documents for Food and Related Products｜Regulations Governing the Management of the Review, Registration and Issuance of Permit Documents for Food and Related Products - Article 2 Food and Drug Administration

  The term “review and registration” herein stated refer to the process of review, test, and registration and the issuance of permit documents. The reg...

  Ministry of Health and Welfare
• Regulations of Inspection of Imported Foods and Related Products｜Regulations of Inspection of Imported Foods and Related Products - Article 2 Food and Drug Administration

  The terms herein are defined as follows: 1. Obligatory Inspection Applicant: A business entity that engaged in the importation of food, genetically m...

  Ministry of Health and Welfare
• REGULATIONS FOR APPLICATION OF HEALTH FOOD PERMIT｜REGULATIONS FOR APPLICATION OF HEALTH FOOD PERMIT - Article 2

  Applications for permit and registration of manufacture and import for health food specified in Subparagraph 1 of Paragraph 1 of Article 3 of the Act...

  Ministry of Health and Welfare
• Rules for Redressing Damage to Farmers Caused by Agricultural Imports｜Rules for Redressing Damage to Farmers Caused by Agricultural Imports - Article 2

  For purposes of these Rules, the “competent authority” shall denote the Council of Agriculture, Executive Yuan.

  農業部
• 農產品受進口損害救助基金收支保管及運用辦法｜農產品受進口損害救助基金收支保管及運用辦法 - Article 2

  本基金為預算法第四條第一項第二款所定之特種基金，隸屬於農業特別收入基金項下，編製附屬單位預算之分預算，以行政院農業委員會為主管機關。

  農業部