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您当前的位置:首页 » 供应产品 » 滁州FDA认证流程?六安GOTS认证现场评估流程介绍?
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滁州FDA认证流程?六安GOTS认证现场评估流程介绍?
发布时间:2020-03-20 18:03        浏览次数:9        返回列表
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品牌:GOTS认证
单价:面议
最小起订量:
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发货期限:自买家付款之日起 3 天内发货
  询价
详细介绍
 AIM
The aim of the standard is to define world-wide recognized requirements that ensure organic status of textiles, from harvesting of the raw materials, through environmentally and socially responsible manufacturing up to labelling in order to provide a credible assurance to the end consumer.
Textile processors and manufacturers are enabled to export their organic fabrics and garments with one certification accepted in all major markets.
目的
标准的目的是定义全球公认的纺织品需求确保有机状态,从原材料的获取,通过环境和社会责任生产标签,以最终消费者提供可靠的保证。
纺织处理器和制造商能有机纺织品和服装出口认证在所有主要市场接受。
 
The consensus of the Founding Organizations was that a clear and unambiguous understanding of the content required that the Global Standard itself focuses on compulsory criteria only. The standard covers the processing, manufacturing, packaging, labelling, trading and distribution of all textiles made from at least 70% certified organic natural fibres. The final products may include, but are not limited to fibre products, yarns, fabrics, clothes and home textiles. The standard does not set criteria for leather products.
标准
成立组织的共识是清晰和明确的理解的内容要求全球标准本身只侧重于强制性标准。标准涵盖的加工、制造、包装、标签、贸易和分销的纺织品制成的至少70%的经过认证的有机天然纤维。最终产品可能包括,但不限于纤维产品、纱线、面料、服装和家用纺织品。皮革制品的标准不标准。
The key criteria for fibre production can be identified as:
Organic certification of fibres on basis of recognised international or national standards (IFOAM family of standards, EEC 834/2007, USDA NOP)
Certification of fibres from conversion period is possible if the applicable farming standard permits such certification
A textile product carrying the GOTS label grade ‘organic’ must contain a minimum of 95% certified organic fibres whereas a product with the label grade ‘made with organic’ must contain a minimum of 70% certified organic fibres
 
 
 
 
FDA 2
 
 
 
 
FDA认证流程:
 
  1.申请方签署《FDA注册报价合同》,填写《FDA注册申请表》;
 
  2.申请方将申请表以及合同盖章后回传我方;
 
  3.环测威发送付款通知;
 
  4.申请方支付注册款项;
 
  5.环测威向FDA办理注册;
 
  6.申请方领取FDA注册相关资料(FDA注册编号、密码、PIN码以及其他相关信息)
 
  7.技术初审申报受理
 
  8. DMF资料审阅
 
  9. FDA检查
 
10.FDA签发“批准信”
 

滁州FDA认证流程?六安GOTS认证现场评估流程介绍?
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