输入邮箱后，选择产品类别和目标市场，我们会为匹配的、经人工核验的更新发送提醒。
Enter your email, then choose your product and market. We’ll send matched, human-reviewed regulatory updates.
回答几个问题，我们的团队会为你准备下一步所需的文件。
Answer a few questions, and our team will prepare the documents you need for the next step.
对话确认产品后要求上传的文件会保存到私密复核案件中，不会进入公开日志、公开数据集或遥测。为改进服务，对话、系统提取的产品事实、结果状态及文件名/类型/大小等上传元数据可能在私密日志中保存最多90天；原始文件和提取正文不会写入该对话日志。请勿上传身份证件、付款资料、密码或无关个人信息。
Files requested after the product conversation are stored privately in the final-review case; they are not placed in public logs, public datasets or telemetry. To improve the service, messages, interpreted facts, result status and filename/type/size metadata may be retained in private conversation logs for up to 90 days; raw files and extracted contents are not written to those conversation logs. Do not upload identity documents, payment data, passwords or unrelated personal information.
提示：亚洲地区的请求可能因跨区域网络和 AI 服务位置而需要更长时间响应。Response times from Asia may be longer because requests may cross regional networks and AI service locations.
按产品和目标市场找出平台可能需要的证据、缺口和下一步。
Identify the evidence, gaps and next step for the product and destination market.
开始免费预检 →Start free preflight →核对UN 38.3摘要是否覆盖该电芯型号和电池组，并整理货代通常索取的文件。
Check whether the UN 38.3 summary covers this exact cell model and pack, and organise the documents a forwarder usually asks for.
核对运输文件 →Check transport documents →对照目标市场复核型号一致性、责任主体信息、必备标志和警示语言。
Review model consistency, responsible-entity details, required symbols and warning language against the destination market.
复核标签稿件 →Review the label artwork →确认适用CPC还是GCC，核对支持性测试证据，并整理报关申报需要的同一批数据。
Work out whether a CPC or GCC applies, check the supporting test evidence, and organise the same data needed at entry.
整理证书与申报数据 →Organise certificate and filing data →把已有证据对照声明需引用的法规和标准，并标出必须确认的字段。
Map the evidence held against the legislation and standards a declaration would cite, and mark the fields that must be confirmed.
复核声明依据 →Review the declaration basis →他们不想先读法规，也不想先买一份模糊的“合规服务”。他们想快速知道：该向供应商要什么、该问实验室什么、哪些表格字段还缺、什么时候必须让人复核。
They do not want to start by reading regulations or buying a vague compliance service. They want to know what to request from the supplier, what to ask a lab, which form fields are missing, and what needs review by our team.
先选择欧盟、美国、英国或澳洲，再根据产品事实生成市场准入准备路径。
Select EU, US, UK or AU first, then generate a readiness route from the product facts.
人工复核会把缺口转成可编辑的供应商邮件、实验室简报、平台材料索引和官方/标准化表格字段草稿；复核人员签字后才发布。
Human review turns gaps into editable supplier emails, lab briefs, marketplace indexes and official/standardised form-field drafts; nothing is released before reviewer sign-off.
文件真实性、型号覆盖、签署主体、实验室范围和最终报告签发都会在人工复核中核对。
Every case proceeds through review of document authenticity, model coverage, signatory identity, lab scope and final sign-off.
同一个案件先解释并保存产品资料，再评估证据准备状态。之后每个案件都必须由我们的团队复核文件和判断点；只有复核人员签字后，才发布下一步资料包。人工复核是本服务的固定阶段，不是另一个产品，也不是可选升级。
The same case first interprets and saves the product profile, then assesses evidence readiness. Mandatory review by our team checks documents and judgement points before the reviewer-signed next-step pack is released. Review is part of the service, not a separate or optional product.
用普通语言描述产品和目标市场。系统提取并保存结构化资料，只询问无法安全推断且会影响路线的事实。
Describe the product and destination in ordinary language. The system extracts and saves a structured profile, asking only for unresolved facts that affect routing.
根据产品资料和已有文件信息生成适用证据、缺口、不确定点、可信度和复核触发点，并在继续前展示结果。
Uses the product profile and known documents to identify applicable evidence, gaps, uncertainties, trust state and review gates, then presents the result before continuing.
阶段二确认后必须先完成人工复核。复核人员签字后，案件才发布供应商补证据、实验室路径、平台提交复核或专项专业复核材料。
Mandatory human review follows Stage 2 confirmation. Only after reviewer sign-off does the case release supplier-evidence, lab, marketplace-review or specialist-referral materials.
卖家补充原始文件后，复核人员核对型号、主体、证据和市场准入判断，并在发布阶段三前签字。
After the seller adds original files, a reviewer checks models, entities, evidence and market-access judgements, then signs off before Stage 3 is released.
阶段三不是单独的检查，也不应跳过前两个阶段。卖家先完成产品资料解释和证据准备状态评估，然后必须由我们的团队复核原始文件、型号覆盖、主体信息和判断点。只有复核人员签字后，同一个案件才发布对应路线、表格字段、邮件和材料索引。
Stage 3 is not a separate check and must not skip the first two stages. After product interpretation and the evidence-readiness assessment, our team must review original files, model coverage, entity details and judgement points. Only reviewer sign-off releases the selected route, form fields, emails and document index for the same case.
生成中英双语供应商文件请求、缺失文件清单、型号/日期/签名一致性检查，并提示不要急着提交给平台或实验室。
Produces Chinese/English supplier evidence requests, exact missing-file lists, model/date/signature consistency checks, and a do-not-submit-yet warning.
生成实验室简报：产品事实、可能适用的测试/技术路径、已有文件、缺失文件和应问实验室的问题。
Builds a lab brief: product facts, likely testing/technical routes, documents held, missing documents, and questions to ask the lab.
当证据包看起来可进入提交准备时，生成文件索引、型号映射表、标签/照片清单、提交顺序和未解决风险备注。
When the package appears ready for submission review, drafts a document index, model mapping table, label/photo checklist, submission order and unresolved risk notes.
当涉及实验室、欧盟责任人、授权代表、进口/海关顾问、监管顾问或律师时，说明升级原因和应发送的证据包。
When a lab, EU/UK responsible person, authorised representative, import adviser, regulatory consultant or lawyer is needed, explains why and what to send.
整理文件索引，对照各文件中的型号，并列出仍未解决的问题——不承诺平台会通过。
Organises a document index, maps model numbers across the files, and lists what is still unresolved — without claiming the listing will pass.
核对UN 38.3摘要是否覆盖该电芯型号、容量和组合方式，整理货代通常索取的文件，并准备向货代确认的问题。
Checks whether the UN 38.3 summary covers this exact cell model, capacity and pack configuration, organises the documents a forwarder usually asks for, and prepares the questions to put to them.
对照目标市场复核标签和包装稿件：型号一致性、责任主体信息、适用的必备标志、警示语言和年龄警示。
Reviews label and packaging artwork against the destination market: model consistency, responsible-entity details, the symbols that apply, warning language and age warnings.
识别适用CPC还是GCC路径并标出分类存疑之处，核对支持性测试证据，整理证书字段和进口商报关申报所需的同一批数据。
Identifies whether the CPC or GCC route applies and flags where that classification is contested, checks the supporting test evidence, and organises the certificate fields and the same data an importer files at entry.
把已有证据对照声明需引用的法规和标准，预填可识别字段，并标出必须由制造商或复核人员确认的内容。
Maps the evidence held against the legislation and standards a declaration would cite, prefills the identifiable fields, and marks what the manufacturer or reviewer must confirm.
路线需要时，同一案件还会附上
Also included in the same case, where the route calls for it
针对仍缺失的具体文件，准备中英双语请求。
Prepares bilingual requests for the specific files still missing.
为实验室整理产品事实、已有证据和待确认的问题。
Organises product facts, evidence held and the open questions for a lab.
适用时，按材料和使用条件整理需要确认的声明信息。
Where it applies, organises declaration information by material and conditions of use.
说明何时需要实验室、责任人、顾问或律师，以及应向他们发送什么。
Explains when a lab, responsible person, adviser or lawyer is needed, and what to send them.
市场准入下一步包是操作草稿，不是认证、法律意见、产品批准或平台通过保证。对外发送前仍应核对产品事实和原始文件。
The Stage 3 pack is a human-reviewed operational deliverable, not certification, legal advice, product approval, or a marketplace approval guarantee. Do not use any provisional Stage 2 output as the final pack.
四类产品在欧盟、英国、美国和澳大利亚均有可用的结构化模块：司法辖区记录、产品问题、证据清单和条件规则。16项司法辖区记录均已核对来源；以下数量和核验状态公开各模块的深度。原始文件仍需复核。
All four product categories have operational structured modules for the EU, UK, US and Australia: a jurisdiction record, product questions, an evidence checklist and conditional rules. All 16 jurisdiction records are source-checked; the counts and review status below show each module’s depth. Original files still require review.
电池、无线电、标签和责任主体资料。
Battery, radio, labelling and operator evidence.
每个市场6–9项证据检查 · 13条条件规则，全部已核对来源6–9 evidence checks/market · 13 conditional rules, all source-checked玩具安全、年龄分级、警示和电池/无线资料。
Toy safety, age grading, warnings and battery/radio evidence.
每个市场8–17项证据检查 · 20条条件规则，全部已核对来源8–17 evidence checks/market · 20 conditional rules, all source-checked配方、安全报告、通报和责任人资料。
Formula, safety report, notification and responsible-person evidence.
每个市场3–7项证据检查 · 11条条件规则，全部已核对来源3–7 evidence checks/market · 11 conditional rules, all source-checked材料、用途、温度和迁移资料。
Material, use conditions, temperature and migration evidence.
每个市场9–13项证据检查 · 24条条件规则，全部已核对来源9–13 evidence checks/market · 24 conditional rules, all source-checked