• Skip to primary navigation
  • Skip to main content
  • Skip to primary sidebar
  • +1-757-224-0177
  • 400-860-0210
  • fdahelpdesk
  • 联系我们
  • MyFDA登录
  • COVID-19 个人防护设备
  • 中文
    • English
    • Español
    • Italiano
    • Deutsch
    • Français
    • Portuguese
    • 日本語
Registrar

Registrar

Assistance with U.S. FDA Regulations

  • 中文
    • English
    • Español
    • Italiano
    • Deutsch
    • Français
    • Portuguese
    • 日本語
  • 向FDA注册
  • 服务
    • 向FDA注册
    • 化妝品FDA註冊
    • 认证及合规培训
    • 食品安全计划和FSMA
    • FDA标签
    • UDI与GUDID
    • 主文件
    • TTB Registration
  • 行业
    • 食品和饮料
    • 膳食补充剂
    • 医疗器械
    • 药品
    • 化妆品
    • 其它
  • 资源
    • 资源
    • 新闻
    • 商业活动/研讨会
    • 工具类
  • 关于我们
    • 关于我们
    • 联系我们

Kosher Certification

Kosher Certification

Registrar Corp has developed a synergetic partnership with Star-K to provide companies with Kosher Certification for their food and beverage products. Star-K is the world’s leading provider in Kosher Certification and has served the Kosher industry for over fifty years.

What is Kosher?

The Kosher food industry is a lucrative and growing market around the world.  Kosher refers to food products that follow Jewish dietary laws. These include rules on how food is prepared as well as what foods or combinations of foods may be consumed. Many other religious or secular diets have similar requirements, providing more demand for foods certified as Kosher.

Why become certified? 

By acquiring certification, your company is letting your customers know that the product is 100% Kosher, and they can buy and consume it with confidence. With an ever growing number of companies producing Kosher food products, certification can help your product stand out by delivering assurance of the legitimacy of your product.

Star-K and Registrar Corp have both been known for their excellent service for many years.  By partnering together, they are providing their clients an all-encompassing solution for Kosher Certification and FDA Compliance for products sold in the United States.

For assistance with Kosher Certification, simply complete the form below:

  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • 提供贵司信息
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • Food Safety

    贵司的食品安全计划符合FDA的要求吗?

    美国FDA要求大多数类型的已注册食品企业建立危害分析和基于风险的预防控制(HARPC)计划。HARPC计划必须遵循美国FDA规定的特定标准。其他食品安全体系可能不能完全满足FDA的要求。

  • Food Safety

    U.S. FDA requires most types of registered food facilities to implement Hazard Analysis and Risk-Based Preventive Controls (HARPC) Plans. A HARPC plan must follow unique standards mandated by U.S. FDA. Other food safety systems may not completely satisfy FDA requirements.

  • Food Label Deadline

    FDA新标签规定的最后期限即将到来

    许多食品公司只有不到XX个月的时间来更新他们的标签,以符合新的FDA标签规则。新规定包括更新营养成分表、食用分量、强制声明等。

  • Food Label Deadline

    出口美国的货物有超过22%的扣货是由于贴标错误导致的。

    在货物被FDA扣留之前,很多企业都不知道他们的产品标签是不符合FDA的要求的。贴标错误兼有可能导致货物被延期,需要重新贴标或者销毁。让Registrar Corp的专家审核贵司的产品标签是否符合FDA的要求可以避免货物到港时因标签不合规导致的高额损失。

  • Drop files here or
    Max. file size: 50 MB.
    • Drop files here or
      Max. file size: 50 MB.
      • 注意: 若没有如下信息Registrar Corp将无法核实贵司的注册状态:

        • 注册号码,以及PIN码;
        • 或
        • 登录FDA系统的用户名和密码。

        若贵司均不知道上述信息,最好立即注册新的号码。

        立即重新注册
      • This field is hidden when viewing the form
      • (11位数号码)
      • (大写字母请指出。)
      • Compliance Information

      •  
      • Drop files here or
        Max. file size: 50 MB.
        • Drop files here or
          Max. file size: 50 MB.
          • Max. file size: 15 MB.
          • Max. file size: 15 MB.
          • Drop files here or
            Max. file size: 15 MB, Max. files: 10.
            • Drop files here or
              Max. file size: 15 MB.
              • Drop files here or
                Max. file size: 15 MB.
                • Drop files here or
                  Max. file size: 15 MB.
                  • Drop files here or
                    Max. file size: 15 MB.

                    • 请为您的每一种获得NIOSH批准的防护口罩提供以下信息
                      生产商名称型号NIOSH批准号 
                    • Drop files here or
                      Max. file size: 50 MB.
                      • 文件/证书应由其他监管机构或者资质评定机构出具。(若有)请提供许可编号以及评定机构名称。
                        Drop files here or
                        Max. file size: 50 MB.
                        •  
                          Drop files here or
                          Max. file size: 50 MB.
                          • 报告应证明产品已经达到相应的性能标准
                            Drop files here or
                            Max. file size: 50 MB.

                            Primary Sidebar

                            联系我们

                             

                            Registrar Corp总部

                            Room 606-608, Block A, Rongchao Binhai

                            Building, No. 5

                            Xinghua 1st Road, Bao’an CBD

                            Shenzhen City, People’s Republic of China

                             

                            400-860-0210

                             

                            (+86)-755-82070866

                             

                            [email protected]

                             
                             
                             
                             

                            查看我们的位置

                            24/7在线帮助

                            我们的方案

                            向FDA注册

                            FDA Compliance Monitor

                            FDA标签

                            查看全部

                            关于我们

                            关于我们

                            资源

                            工具

                            费用

                            联系我们

                             

                            评论

                            地址

                            商业活动

                            协会

                            电话: +1-757-224-0177

                            传真: +1-757-224-0179

                            [email protected]

                            © 2025 Registrar Corp

                            144 Research Drive Hampton, Virginia 23666 USA
                            使用条款 | 隐私条例

                            • 中文
                              • English
                              • Español
                              • Italiano
                              • Deutsch
                              • Français
                              • Portuguese
                              • 日本語
                              • Back
                            • 向FDA注册
                            • 服务
                              • 向FDA注册
                              • 化妝品FDA註冊
                              • 认证及合规培训
                              • 食品安全计划和FSMA
                              • FDA标签
                              • UDI与GUDID
                              • 主文件
                              • TTB Registration
                              • Back
                            • 行业
                              • 食品和饮料
                              • 膳食补充剂
                              • 医疗器械
                              • 药品
                              • 化妆品
                              • 其它
                              • Back
                            • 资源
                              • 资源
                              • 新闻
                              • 商业活动/研讨会
                              • 工具类
                              • Back
                            • 关于我们
                              • 关于我们
                              • 联系我们
                              • Back

                            通知:未能完成 年FDA注册续期的企业必须重新注册

                            通知: 未能完成 年医疗器械FDA注册和药品FDA注册续期的企业必须重新注册

                            立即重新注册

                            已持有FDA注册的企业必须在 年12月31日前延续其注册

                            医疗器械注册和药品注册必须在 年12月31日前完成注册续期

                            立即续期

                            提醒

                            美国食品药品管理局(FDA)要求所有食品、药品、 医疗器械注册企业在 年10月1日到12月31日期间延续其注册。

                            立即续期

                            通知

                            美国FDA注册延续时间将在年12月31日截至

                            若您未能在截止日前完成续期,将需要重新注册。

                            重新注册或者验证您的注册是否已延续至:

                            重新注册
                            验证

                            限时特惠

                            即日注册,即可用一年的费用享受18个月的注册和代理人服务有效期

                            Get Started