fda对于美代这块，管理越来越严格的，以往很多企业找客户、找朋友 或者找一些便宜的个人或者检测公司做为自己的美代公司，但是现在的话fda越到问题或者客户有问题基本都是直接与美国代理人这边直接沟通处理的 所以如果出现此类问题，建议尽快更换美代，不要影响企业fda注册以及产品出口 选择的美国代理人 选择了sungo作为美代的您可以享受到如下星级服务： 1. fda注册的日常维持，更新； 2. fda新动态的时间告知及建议； 3. 随时为您提供与fda注册和上市后监管等相关的事务的处理意见； 4. 可代表您回答您美国客户的相关fda问题（英文邮件，英文电话会议均可）； 5. 接受fda验厂时，以优惠的价格提供qsr820、审核经验传授及全程英语陪审
responsibilities of a u.s. agent the u.s. agent must either reside in the u.s. or maintain a place of business in the u.s. the u.s. agent cannot use a post office box as an address. the u.s. agent cannot use an answering service. they must be available to answer the phone or have an employee available to answer the phone during normal business hours. the responsibilities of the u.s. agent are limited and include: assisting fda in communications with the foreign establishment, responding to concerning the foreign establishment's devices that are imported or offered for import into the united states, assisting fda in scheduling inspections of the foreign establishment and if fda is unable to contact the foreign establishment directly or expeditiously, fda may provide information or documents to the u.s. agent, and such an action shall be considered to be e to providing the same information or documents to the foreign establishment. please note that the u.s. agent has no responsibility related to reporting of adverse events under the medical device reporting regulation (21 cfr part 803), or submitting 510(k) premarket notifications (21 cfr part 807, subpart e).
fda对于美国代理人的解释也可以参考看一下网站的原文： any foreign establishment engaged in the manufacture, preparation, propagation, compounding, or processing of a device imported into the united states must identify a united states agent (u.s. agent) for that establishment. information about a foreign establishment’s u.s. agent is submitted electronically using the fda unified registration and listing system (furls system) and is part of the establishment registration process. each foreign establishment may designate only one u.s. agent. the foreign establishment may also, but is not required to, designate its u.s. agent as its official correspondent. the foreign establishment should provide the name, address, telephone and fax numbers, and e-mail address of the u.s. agent. the u.s. agent identified will be required to complete an automated process to confirm that they have agreed to act as the u.s. agent. the automated process will forward an email verification request to the u.s. agent. they will be re to confirm her/his consent to act as a representative/liaison on behalf of the foreign establishment. if the u.s. agent denies consent (or does not respond within 10 business days), the official correspondent/owner operator of the foreign establishment will be notified and must designate a new u.s. agent to satisfy the regulatory obligation.
化妆品fda注册 fda化妆品注册 1/ 化妆品企业注册可以在出口美国之前或者出口之后（30天内）； 2/ 化妆品产品注册需要有1000美金的出口之后，但是实际上fda无法核对； 3/ can i file formulations in the vcrp for products that are considered drugs but also have a cosmetic function? 对于药品有化妆品功能的是否可以做化妆品注册？ yes, products that are considered drugs in the united states, such as sunscreens, but also make cosmetic type claims, such as moisturizing, can be filed in the vcrp. 4/ 可以进行化妆品注册，但是这并不能豁免其需要同时满足药品的相关要求的职责。 办理化妆品的fda相对来说比较简单，企业提供企业信息以及产品成分表（中英文）就可以了。
fda注册的流程 1）提供贵公司产品信息，我司为你进行产品类别判定并确定申请路径； 2）贵公司提供公司信息和产品信息，中英文信息，依据我司提供的申请表格式； 3）签署合约，同时美国代理人协议签署和生效； 4）我司协助申请贵公司支付美金到美国fda； 5）我司提交注册申请资料给美国fda审批； 6）注册审批完成，获得批准号码； 7）我司颁发证书； 8）次年开始进行年度更新注册。
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