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Drug Administration

Drug Administration, Total:59 items.

In the international standard classification, Drug Administration involves: HEALTH CARE TECHNOLOGY, Pharmaceutics, Services, Vocabularies, Food products in general, Postal services, Quality.

IX-EU/EC, Drug Administration

• 89/341/EEC-1989 Council Directive Amending Directives 65/ 65/EEC, 75/318/EEC and 75/319/EEC on the Approximation of Provisions Laid Down by Law, Regulation or Administrative Action Relating to Proprietary Medicinal Products
• 87/21/EEC-1986 Council Directive Amending Directive 65/ 65/EEC on the Approximation of Provisions Laid Down by Law, Regulation or Administrative Action Relating to Proprietary Medicinal Products
• 65/65/EEC-1996 Council Directive of 26 January 1965 on the Approximation of Provisions Laid Down by Law, Regulation or Administrative Action Relating to Proprietary Medicinal Products ((Amended by 87/21/EEC 89/341/EEC, 93/39/EEC, and COM(88) 663))
• 85/432/EEC-1985 Council Directive Concerning the Coordination of Provisions Laid Down by Law, Regulation or Administrative Action in Respect of Certain Activities in the Field of Pharmacy

US-CFR-file, Drug Administration

• CFR 21-800.55-2014 Food and Drugs. Part800:General. Section800.55:Administrative detention.
• CFR 21-1.980-2014 Food and drugs. Part1:General enforcement regulations. SubpartQ:Administrative detention of drugs intended for human or animal use. Section1.980:Administrative detention of drugs.
• CFR 40-168.69-2013 Protection of Environment. Part168:Statements of enforcement policies and interpretations. Section168.69:Registered export pesticide products.
• CFR 40-168.69-2014 Protection of Environment. Part168:Statements of enforcement policies and interpretations. Section168.69:Registered export pesticide products.
• CFR 21-10.90-2014 Food and drugs. Part10:Administrative practices and procedures. SubpartB:General administrative procedures. Section10.90:Food and Drug Administration regulations, recommendations, and agreements.
• CFR 40-168.70-2013 Protection of Environment. Part168:Statements of enforcement policies and interpretations. Section168.70:Unregistered export pesticide products.
• CFR 40-168.70-2014 Protection of Environment. Part168:Statements of enforcement policies and interpretations. Section168.70:Unregistered export pesticide products.
• CFR 21-10.85-2014 Food and drugs. Part10:Administrative practices and procedures. SubpartB:General administrative procedures. Section10.85:Advisory opinions.
• CFR 27-555.25-2014 Alcohol, Tobacco Products and Firearms. Part555:Commerce in explosives. SubpartC:Administrative and Miscellaneous Provisions. Section555.25:Disclosure of information.
• CFR 27-555.21-2014 Alcohol, Tobacco Products and Firearms. Part555:Commerce in explosives. SubpartC:Administrative and Miscellaneous Provisions. Section555.21:Forms prescribed.
• CFR 40-168.66-2013 Protection of Environment. Part158:Data requirements for pesticides. Section168.66:Labeling of pesticide products and devices intended solely for export.
• CFR 40-168.66-2014 Protection of Environment. Part168:Statements of enforcement policies and interpretations. Section168.66:Labeling of pesticide products and devices intended solely for export.
• CFR 40-168.71-2013 Protection of Environment. Part168:Statements of enforcement policies and interpretations. Section168.71:Export pesticide devices.
• CFR 40-168.71-2014 Protection of Environment. Part168:Statements of enforcement policies and interpretations. Section168.71:Export pesticide devices.
• CFR 27-478.21-2014 Alcohol, Tobacco Products and Firearms. Part478:Commerce in firearms and ammunition. SubpartC:Administrative and Miscellaneous Provisions. Section478.21:Forms prescribed.
• CFR 14-1204.1005-2013 Aeronautics and space. Part1204:Administrative authority and policy. Section1204.1005:Unauthorized introduction of firearms or weapons, explosives, or other dangerous materials.
• CFR 21-1.1-2013 Food and Drugs. Part1:General enforcement regulations. Section1.1:General.
• CFR 21-10.95-2014 Food and drugs. Part10:Administrative practices and procedures. SubpartB:General administrative procedures. Section10.95:Participation in outside standard-setting activities.
• CFR 21-21.52-2014 Food and drugs. Part21:Protection of privacy. SubpartE:Procedures for requests for amendment of records. Section21.52:Administrative appeals of refusals to amend records.

Professional Standard - Pharmaceutical Packaging, Drug Administration

• YBB 0015(02)-2002 Aluminum foil for pharmaceutical packaging (trial implementation)
• YBB 0013(02)-2002 General Rules for Composite Films and Bags for Pharmaceutical Packaging (Trial)
• YBB 0014(02)-2002 Guidelines for Compatibility Testing of Drug Packaging Materials and Drugs (Trial)

GB-REG, Drug Administration

• REG 7 CFR PART 279-2012 ADMINISTRATIVE AND JUDICIAL REVIEW - FOOD RETAILERS AND FOOD WHOLESALERS

CO-ICONTEC, Drug Administration

• ICONTEC 1.565-1980

Group Standards of the People's Republic of China, Drug Administration

• T/JXYXH 0002-2022 Specification for product release of drug?manufacturing?enterprise
• T/JXYXH 0003-2022 Specification for material release of drug?manufacturing?enterprise
• T/CACM 1021.183-2018 Product Specifications and Grades of Chinese Medicinal Materials Wangbuliuxing
• T/YAIMH 001-2022 Regulations for the management of high-alert drugs in Internet hospitals

Shanghai Provincial Standard of the People's Republic of China, Drug Administration

• DB31/T 1443-2023

Professional Standard - Environmental Protection, Drug Administration

• HJ 1256-2022 Technical guidelines for self-monitoring of pollutant discharge units

US-HHS, Drug Administration

• HHS 21 CFR PART 211-2011 CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS
• HHS 21 CFR PART 226-2011 CURRENT GOOD MANUFACTURING PRACTICE FOR TYPE A MEDICATED ARTICLES

US-FCR, Drug Administration

• FCR 21 CFR PART 211-2015 CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS
• FCR 21 CFR PART 211-2014 CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS
• FCR 21 CFR PART 211-2013 CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS
• FCR 21 CFR PART 226-2015 CURRENT GOOD MANUFACTURING PRACTICE FOR TYPE A MEDICATED ARTICLES
• FCR 21 CFR PART 226-2013 CURRENT GOOD MANUFACTURING PRACTICE FOR TYPE A MEDICATED ARTICLES

Tianjin Provincial Standard of the People's Republic of China, Drug Administration

• DB12/T 732-2017 Tianjin Municipal Administrative Licensing Items Operating Procedures for Petroleum Refined Oil
• DB12/T 659-2016 Operating Procedures for Tianjin Administrative Licensing Items Commodity Housing Sales Licensing

Zhejiang Provincial Standard of the People's Republic of China, Drug Administration

• DB3301/T 0343.4-2021 Food Production Safety Supervision Guidelines Part 4 Administrative Guidance
• DB3301/T 0343.2-2021 Food Production Safety Supervision Guidelines Part 2 Administrative Supervision

Professional Standard - Business, Drug Administration

• SB/T 10765-2012 Standard for professional managers of pharmaceutical distribution industry

Guangdong Provincial Standard of the People's Republic of China, Drug Administration

• DB44/T 767-2010 Social Responsibility of Food and Pharmaceutical Industry in Guangdong Province
• DB44/T 766-2010 Guangdong province food and medicine industry self-discipline management norms

Professional Standard - Postal Service, Drug Administration

• YZ/T 0005.3-2002 Postal service vocabulary Part 8:postage item issue and philately

Korean Agency for Technology and Standards (KATS), Drug Administration

• KS J 0022-2010 Laboratory control system policy in biopharmaceutical production based on Good Manufacturing Practice
• KS J 0017-2010 Quality system policy in biopharmaceutical production based on Good Manufacturing Practice

British Standards Institution (BSI), Drug Administration

• BS PD CEN/TR 17612:2021 Algae and algae products. Specifications for pharmaceutical sector applications

AT-ON, Drug Administration

• ONR CEN/TR 17612-2021 Algae and algae products - Specifications for pharmaceutical sector applications

Danish Standards Foundation, Drug Administration

• DS/CEN/TR 17612:2021 Algae and algae products – Specifications for pharmaceutical sector applications

Professional Standard - Agriculture, Drug Administration

• 65兽药典 二部-2015 Product Name Catalog Medicinal Materials and Pieces Four Paintings Wangbuliuxing
• 食药监办食监三函〔2014〕235号 Reply Letter from the General Office of the China Food and Drug Administration on the Qualification of the Illegal Addition of Drugs Phenolphthalein and Fluoxetine

European Committee for Standardization (CEN), Drug Administration

• PD CEN/TR 17612:2021 Algae and algae products - Specifications for pharmaceutical sector applications

ES-UNE, Drug Administration

• UNE-CEN/TR 17612:2022 IN:2022 Algae and algae products - Specifications for pharmaceutical sector applications

German Institute for Standardization, Drug Administration

• DIN 11854:2015-09 Components for the food and pharmaceutical industry - Hose unions of stainless steel

Others:   administrative, administrative security, law enforcement, water administration, Administration, water administration, administrative fee, Administrative plan, Drug Administration, Administrative Assistant, Administrative License, administrative definition, administrative fee, administrative services, Administrative penalties, administrator, administrative processing, law enforcement, executive power, Administrative Reconsideration.