Before You Read
- Check the report or certificate number exactly as shown on the issued document.
- Compare the public verification status with the document version and issue information.
- Prepare product information and platform notices when requesting document review support.
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Common Components of Public Verification Information
Public verification information on test reports or compliance documents typically includes the following:
– Report Number: Used for internal management and matching file versions when uploading to platforms.
– Product Name and Model: Must be consistent with the platform listing to avoid additional inquiries due to name discrepancies.
– Test Standards/Regulation Numbers: For example, EN 71, ASTM F963, FCC Part 15, REACH (EC) No 1907/2006, etc.
– Test Items and Results: Clearly indicate pass/fail status; some platforms require specific numerical values.
– Issue Date and Validity (if applicable): Some reports may indicate a suggested retest interval, but actual usability depends on regulations, product changes, and platform rules.
– Laboratory Information: Includes name, address, and scope of accreditation (e.g., CNAS, A2LA, FCC-recognized TCB, etc.). When verifying, ensure the laboratory’s accreditation covers the declared test standards.
How to Verify Report Numbers and Platform Upload Requirements
The report number is generally assigned by the laboratory and serves as a field for locating the document. Platforms often require the report number to be entered for backend verification. Recommended actions:
– Ensure the report number is complete and matches the paper or PDF file.
– If the platform requires uploading a PDF and manually entering the number, copy it accurately to avoid case or character errors.
– Different platforms may have varying format requirements for report numbers; some only accept alphanumeric combinations. Follow platform instructions.
Note: The report number alone cannot serve as the sole basis for authenticity verification. Regulatory bodies or platforms may further verify laboratory qualifications and report validity through public query channels, but not all reports provide public query access.
Report Status and Coverage Scope
To determine whether a report is still applicable to the current product, consider the following:
– No changes to the product: Changes in materials, processes, suppliers, key components, etc., may affect test results and require an updated report.
– No updates to regulations/standards: If applicable standards have been revised, older reports may not be accepted. For example, when toy chemical testing transitions from the old EN 71-3 to the new version, platforms may request supplementary testing for differences.
– Product coverage in the report: Some reports cover a series of models, but verify that the model range listed on the report includes the actual products being sold.
Common Misconceptions About Report Verification
Misconception 1: All reports can be queried publicly online.
Not all laboratories provide online query functions, especially those issued by non-accredited laboratories. Even if a query is available, the results must match the held report.
Misconception 2: Same report number means complete authenticity.
The report number can be a starting point for verification, but it does not rule out misuse. It is recommended to also check laboratory name, standard numbers, product information, and other key fields.
Misconception 3: Fixed validity period means the report is completely invalid after expiration.
Except for specific regulatory requirements (e.g., REACH controlled substance annual updates) or platform-specific rules, most reports do not have a fixed validity period. Whether they can still be used for review depends on product changes, regulatory status, and platform rules, not simply an “expiration” judgment.
Pre-Submission Document Checklist
- Verify that the report number is clearly readable and matches the document.
- Check that product name and model exactly match the platform listing.
- Confirm that the test standards are the latest version (if applicable).
- Confirm that the laboratory accreditation covers the declared test standards (e.g., CNAS, A2LA, FCC TCB, etc.).
- Organize all compliance documents (test reports, DoC, CPC document, FCC authorization records, etc.) and categorize them.
- Retain platform rejection screenshots to facilitate supplementary submissions or re-uploads.
Risk Notice
Platforms retain the final authority to verify reports. This article provides document preparation and verification approaches only and does not constitute a guarantee of platform acceptance. Product category, target market, applicable regulations, and platform rules may all affect review outcomes. It is recommended to fully understand the latest platform requirements and consult with professional testing and certification organizations during preparation.
Pre-Submission Checklist
- Report or certificate number
- Product name, model and applicant information
- Issue date and applicable standard shown on the document
- Platform notice, QR code screenshot or document submission request when available
Public verification results are for document status checking only. Platform review outcomes depend on product information, applicable requirements and the platform review process.
Article FAQ
Are the report number and certificate number the same?
Not necessarily. Some test reports only provide a report number, while certificates (e.g., CE DoC, FCC authorization) may have a separate certificate number. When uploading, follow the platform requirements for the corresponding field.
Can a report be used if the product model on the report does not exactly match the platform listing?
It depends on the platform rules. Some platforms require an exact match; otherwise, they may request additional explanation documents. It is recommended to describe the model relationship in the product description or remarks, or contact the platform customer service for confirmation.
What if the laboratory information on the report does not match the query website?
First check the official name of the laboratory that issued the report. If inconsistent, contact the laboratory to confirm whether it is a typographical error or an authorization change. Some laboratories may have changed their name or accreditation, requiring a change explanation document.
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