Legal Regulations

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

Showing 20 / 34812 legal regulations

• The Regulations on Collection,Custody and Use of Commercial Port Dues｜The Regulations on Collection,Custody and Use of Commercial Port Dues - Article 1

  The said Regulations are enacted in accordance with paragraph 2 of Article 12 of the Commercial Port Law (hereafter cited as "this Law")

  交通部
• Regulations of Civil Air Transport Enterprise｜Regulations of Civil Air Transport Enterprise - Article 1 航空

  This Regulations is enacted in accordance with Article 63-1 of the Civil Aviation Act (hereinafter referred to as The Act).

  交通部
• Regulations Governing General Aviation｜Regulations Governing General Aviation - Article 1

  This Regulation is enacted in accordance with the terms in Paragraph 2 of Article 64-1 of the Civil Aviation Act (hereafter referred to as this Act.)

  交通部
• Regulations Governing Air Cargo Entrepots｜Regulations Governing Air Cargo Entrepots - Article 1

  This Regulation is enacted in accordance with the first paragraph of Article 72-1, Civil Aviation Act.

  交通部
• Regulations Governing the Certification for Aviation Products, Appliances and Parts｜Regulations Governing the Certification for Aviation Products, Appliances and Parts - Article 1 航空

  The Regulations are established pursuant to the provisions of Paragraph 4, Article 9 of the Civil Aviation Act.

  交通部
• Aircraft Flight Operation Regulations｜Aircraft Flight Operation Regulations - Article 1 航空

  This regulation is established in accordance with Article 41-1, paragraph 2 of the Civil Aviation Act (the “Act”).

  交通部
• Regulations for the Custody and Utilization of Revenues and Expenditures of the Operation Fund of the Pharmaceutical Plant of Controlled Drugs｜Regulations for the Custody and Utilization of Revenues and Expenditures of the Operation Fund of the Pharmaceutical Plant of Controlled Drugs - Article 1

  The Operation Fund of the Pharmaceutical Plant of Controlled Drugs (hereinafter referred to as the “Fund”) is established for the purpose of handling...

  Ministry of Health and Welfare
• Regulations for the Assessment and Approval Process of Hazardous Medical Device｜Regulations for the Assessment and Approval Process of Hazardous Medical Device - Article 1

  The Guideline is stipulated pursuant to Paragraph 3, Article 93 of the Medical Care Act (hereinafter referred to as the Act).

  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 1

  本辦法依身心障礙者權益保障法（以下簡稱本法）第六條第三項規定訂定之。

  Ministry of Health and Welfare
• Pharmaceutical Affairs Act Enforcement Rules｜Pharmaceutical Affairs Act Enforcement Rules - Article 1

  These Enforcement Rules are adopted pursuant to Article 105 of the Pharmaceutical Affairs Act ("the Act").

  Ministry of Health and Welfare
• Regulations on Management of Medicament Samples and Gifts｜Regulations on Management of Medicament Samples and Gifts - Article 1

  These Regulations are established in accordance with the stipulations of the Pharmaceutical Affairs Act (hereafter referred as the Act), Article 55, P...

  Ministry of Health and Welfare
• Regulations of Medicament Manufacturer Inspection｜Regulations of Medicament Manufacturer Inspection - Article 1

  This set of regulations is formulated in accordance with regulations of Paragraph 3, Article 71 of the Pharmaceutical Affairs Act.

  Ministry of Health and Welfare
• Enforcement Rules for the Controlled Drugs Act｜Enforcement Rules for the Controlled Drugs Act - Article 1

  These Enforcement Rules are issued in accordance with Article 43 of the Controlled Drugs Act (hereinafter "this Act").

  Ministry of Health and Welfare
• Enforcement Rules of Cosmetic Hygiene and Safety Act｜Enforcement Rules of Cosmetic Hygiene and Safety Act - Article 1

  This rule (the “Rule”) is enacted per Article 31 of Cosmetic Hygiene and Safety Act (the “Act”).

  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 1

  本辦法依罕見疾病防治及藥物法第二十五條規定訂定之。

  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 1

  本辦法依罕見疾病防治及藥物法（以下簡稱本法）第十九條第三項及第二十二條規定訂定之。

  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 1

  本準則依罕見疾病防治及藥物法（以下簡稱本法）第十五條及第二十二條之規定訂定之。

  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 1

  本準則所稱之「人用血漿製劑」，係指將多袋人血漿混合（pooling）、分層（Fractionation）精製而得之治療性產品。於某些情況下，亦可篩檢出含高力價特定抗體之人...

  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 1

  體外診斷藥物係指用來診斷疾病或在判定治療前、治療中、預防疾病或疾病復發等健康狀況所用之生物藥品、醫療器材或其他工具（如：電腦軟體等）。本基準所稱之「生...

  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 1

  本基準所稱之「疫苗類藥品」，係指由免疫抗原組成的藥品，經由人體投與後可刺激免疫系統，對疾病或感染源產生預防、改善或治療的效果。 一 「疫苗」的組成包括...

  Ministry of Health and Welfare