通报号: G/SPS/N/USA/2772
ICS号: 67
发布日期: 2015-08-05
截至日期: 2015-07-29
通报成员: 美国
目标和理由: 保障食品安全
内容概述: 食品和药物管理局(FDA)宣布可提供一项题为“乳和乳制品内兽药残留风险管理多重标准排序模式”的风险评估。该风险评估是有助于对应纳入乳检测计划的兽药残留进行再评估工具。食品药物管理局特承接本项目,以回应州际乳运输全国会议(NCIMS)的要求。
通报热点:农兽药残留
正文:
世界贸易组织 |
G/SPS/N/USA/2772
2015-08-05
15-4037
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卫生及植物卫生措施委员会 |
原文:英文
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通 报
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通报成员: 美国
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负责机构:美国食品和药物管理局(FDA)
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覆盖的产品: HS代码: 04; ICS代码: 67;乳和乳制品
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可能受影响的地区或国家: 所有贸易伙伴
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通报标题: 乳和乳制品内兽药残留风险管理的多重标准排序模块;可提供通知:
语言:英文 页数:2页 链接网址:
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内容简述:食品和药物管理局(FDA)宣布可提供一项题为“乳和乳制品内兽药残留风险管理多重标准排序模式”的风险评估。该风险评估是有助于对应纳入乳检测计划的兽药残留进行再评估工具。食品药物管理局特承接本项目,以回应州际乳运输全国会议(NCIMS)的要求。
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目标与理由:食品安全
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与国际标准不符之处及原因: 无
该法规草案是否符合相关国际标准: 符合标准
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拟批准日期:不适用
拟公布日期:不适用
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拟生效日期: 不适用
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意见反馈截止日期: 2015年7月29日
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负责处理反馈意见的机构: 相关人士可提交电子版风险评估相关评议发送至: http://www.regulations.gov/ ,或书面评议提交至 DivisionofDocketsManagement(HFA-305), FoodandDrugAdministration, 5630FishersLane,Rm.1061, Rockville,MD20852. 只需提交一份评议。表明评议相关文档号:FDA-2015-N-1305.
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文本可从以下机构得到: 国家通报机构 UnitedStatesSPSNationalNotificationAuthority, USDAForeignAgriculturalService, InternationalRegulationsandStandardsDivision(IRSD), Stop1014,WashingtonD.C.20250; Tel:+(1202)7201301; Fax:+(1202)7200433; E-mail:us.spsenquirypoint@fas.usda.gov 另联邦纪事,80册,83号,24260页提供全文,或: http://www.gpo.gov/fdsys/pkg/FR-2015-04-30/pdf/2015-10000.pdf
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正文(英):
NOTIFICATION
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Notifying Member: United States of America
If applicable, name of local government involved:
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Agency responsible: US Food and Drug Administration
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Products covered (provide tariff item number(s) as specified in national schedules deposited with the WTO; ICS numbers should be provided in addition, where applicable): HS Code(s): 04; ICS Code(s): 67 Milk and milk products
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Regions or countries likely to be affected, to the extent relevant or practicable:
[X] All trading partners
[ ] Specific regions or countries:
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Title of the notified document: Multicriteria-Based Ranking Model for Risk Management of Animal Drug Residues in Milk and Milk Products; Notice of Availability Language(s): English Number of pages: 2
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Description of content: The Food and Drug Administration (FDA) is announcing the availability of a risk assessment entitled "Multicriteria-Based Ranking Model for Risk Management of Animal Drug Residues in Milk and Milk Products". The risk assessment is a tool to assist with re-evaluating which animal drug residues should be included in milk testing programs. FDA undertook this project in response to a request from the National Conference on Interstate Milk Shipments (NCIMS).
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Objective and rationale: [X] food safety, [ ] animal health, [ ] plant protection, [ ] protect humans from animal/plant pest or disease, [ ] protect territory from other damage from pests.
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Is there a relevant international standard? If so, identify the standard:
[ ] Codex Alimentarius Commission (e.g. title or serial number of Codex standard or related text)
[ ] World Organization for Animal Health (OIE) (e.g. Terrestrial or Aquatic Animal Health Code, chapter number)
[ ] International Plant Protection Convention (e.g. ISPM number)
[X] None
Does this proposed regulation conform to the relevant international standard?
[ ] Yes [ ] No
If no, describe, whenever possible, how and why it deviates from the international standard:
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Other relevant documents and language(s) in which these are available:
1. FDA Webpage: Multicriteria-based Ranking Model for Risk Management of Animal Drug Residues in Milk and Milk Products
http://www.fda.gov/Food/FoodScienceResearch/RiskSafetyAssessment/ucm443549.htm
2. Multicriteria-Based Ranking Model for Risk Management of Animal Drug Residues in Milk and Milk Products
http://www.fda.gov/downloads/Food/FoodScienceResearch/RiskSafetyAssessment/UCM444035.pdf (available in English)
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Proposed date of adoption (dd/mm/yy): Not applicable
Proposed date of publication (dd/mm/yy): Not applicable
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Proposed date of entry into force: [ ] Six months from date of publication, and/or (dd/mm/yy): Not applicable
[ ] Trade facilitating measure
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Final date for comments: [ ] Sixty days from the date of circulation of the notification and/or (dd/mm/yy): 29 July 2015
Agency or authority designated to handle comments: [ ] National Notification Authority, [ ] National Enquiry Point. Address, fax number and e?mail address (if available) of other body:
Interested persons may submit comments regarding the risk assessment either electronically to http://www.regulations.gov/ or in writing to the Division of Dockets Management (HFA-305), Food and Drug Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852. It is only necessary to send one set of comments. Identify comments with docket number FDA-2015-N-1305.
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Text(s) available from: [X] National Notification Authority, [ ] National Enquiry Point. Address, fax number and e?mail address (if available) of other body:
United States SPS National Notification Authority, USDA Foreign Agricultural Service, International Regulations and Standards Division (IRSD), Stop 1014, Washington D.C. 20250; Tel: +(1 202) 720 1301; Fax: +(1 202) 720 0433; E-mail: us.spsenquirypoint@fas.usda.gov
Text can be also be found in the Federal Register, Vol. 80, No. 83, Page 24260 or on the Internet at: http://www.gpo.gov/fdsys/pkg/FR-2015-04-30/pdf/2015-10000.pdf
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