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.
ContentsTap to expand or collapse
- Basic Information to Prepare Before Applying for Testing and Certification
- Company Details – How to Fill in Applicant Information
- Product Details – Model, Specifications, Intended Use and Applicable Standards
- Key Elements of Labels, Instructions and Image Materials
- Can Existing Reports Be Reused in a New Application?
- Common Document Gaps and Suggested Responses
- Pre-Submission Checklist
- Related Services and Professional Support
1. Basic Information to Prepare Before Applying for Testing and Certification
Before filling in a test and certification application form, it is recommended to organize the following basic information:
Company details: Business license (in English and Chinese), contact person, contact information, factory address (if multiple production sites exist, provide each separately).
Product details: Product name, model, batch number, main materials/components, intended use description, target market (e.g., EU, USA, UK).
Technical documents: Circuit diagrams, instructions, risk assessment records (if applicable).
Existing compliance documents: Previous test reports, certificates, declarations of conformity (DoC), FCC authorization records, etc.
Sample information: Whether sample shipment is required, quantity of samples, any special labeling needed. The above information directly affects the accuracy and review efficiency of the application form.
2. Company Details – How to Fill in Applicant Information
The application form may requests the legal name, registered address, contact person and email of the applicant. Please note:
• The brand owner or manufacturer should be consistent with the legal entity registered on the platform.
• If a third-party laboratory is engaged, the authorization relationship should be clearly stated and a letter of authorization (LOA) attached.
• In multi-entity or OEM/ODM scenarios, it is recommended to clarify the actual manufacturer and designer. Some regulations (e.g., FDA, FCC) require consistency of responsible party information. Do not use abbreviations or phonetic names in place of the business registration name, as this may lead to document rejection during platform review.
3. Product Details – Model, Specifications, Intended Use and Applicable Standards
Product details form the core of the application form. Common fields include:
Product name and model: Must be exactly the same as on the product label; do not use arbitrary abbreviations.
Main technical parameters: Voltage, power, dimensions, materials, etc. (varies by product category).
Intended use: e.g., “household”, “children’s use”, “outdoor” – this directly affects applicable regulations (e.g., toys may need to consider EN71 / CPSC or applicable product safety authorities or market surveillance authorities, electronic equipment may need EMC/LVD).
Applicable standards: e.g., harmonized standards under CE marking, FCC Part 15, ASTM F963, etc. It is recommended to select based on actual product functions to avoid omission or over-extension. During platform review, these details are typically checked against the submitted reports and labels.
4. Key Elements of Labels, Instructions and Image Materials
Many platforms require the simultaneous submission of product labels, instructions and actual photos when reviewing compliance documents. Corresponding sections in the application form typically need:
• Brand, model, country of origin, warnings (if applicable, such as CE mark, UKCA mark, FCC mark) on labels.
• Safety instructions, age warnings, compliance statements in the instruction manual.
• Multi-angle product photos (including packaging, nameplate, battery compartment, etc.).
Ensure all printed information matches what is filled in the application form. If language requirements exist (e.g., German, French), provide corresponding translations.
5. Can Existing Reports Be Reused in a New Application?
Some test and certification application forms may ask whether there are previous test reports or certificates. You need to evaluate:
• Whether the report is still valid (different regulations/standards have different validity periods; no uniform duration applies).
• Whether the product has undergone any design, material or process changes.
• Whether the test items covered by the report still meet current target market requirements.
If an existing report is fully consistent with the current product and the standard has not been updated, some data may be reused. However, platforms may request the full original report rather than a summary on the application form. It is recommended to honestly fill in the original report number and issuing body information, and attach a copy of the report for review by the laboratory or platform.
6. Common Document Gaps and Suggested Responses
Based on service experience, the following document gaps occur frequently in application forms:
• Missing intended use description or target market clarification, leading to uncertainty about applicable standards.
• Applicant name inconsistent with business license, or missing LOA (letter of authorization).
• Labels missing required compliance marks or warnings, e.g., CE mark, UKCA mark, FCC mark, age warnings.
• Existing reports do not cover all product models or batches.
• Sample information unclear, not distinguishing between normal samples and auxiliary samples.
To address these issues, it is recommended to verify each item when filling in the application form and contact the laboratory or compliance consultant if necessary.
7. Pre-Submission Checklist
Before submitting a test and certification application form, confirm the following:
1. Company information matches the entity registered on the platform.
2. Product name, model and batch number exactly match the labels.
3. Applicable standards correctly selected (based on product category and target market).
4. Sufficient samples and test conditions available.
5. Existing reports still applicable, and whether authorization or declaration needs to be attached.
6. Label and instruction photos are complete and clear.
7. Latest platform compliance requirements reviewed (e.g., Amazon, TEMU, TikTok Shop rules may be updated).
8. For high-risk products (e.g., children’s products, medical devices, wireless transmitting devices), whether additional documents may be requested (e.g., CPC document, FCC TCB authorization letter).
Final platform review results are subject to platform rules, product information and the actual submitted materials. This checklist is for reference only.
8. Related Services and Professional Support
If you are unsure how to fill in a test and certification application form, or need assistance organizing company details, product technical documents and label compliance, our compliance consultant team can provide the following support:
• Develop a document checklist and guidance specifically for your product.
• Help analyze platform rejection reasons and provide modification suggestions.
• Arrange pre-evaluation and sample testing with partner laboratories.
Please feel free to download a reference template for test and certification application forms, or contact us directly for one-on-one consultation.
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
Must the product model filled in on the application form be exactly the same as on the label?
It is recommended to be completely consistent. If there are multiple variants (e.g., different colors or sizes), you may fill in a series of models and explain in the remarks, but the core model number should correspond to the label and test report.
Can a single application form cover multiple target markets?
Yes, but you need to check or specify applicable regulations and standards for each market (e.g., applying for both CE and UKCA). Note that different markets may have differing requirements (e.g., voltage, plug type, restricted substances). It is recommended to confirm with the laboratory in advance whether test items can be combined to reduce costs.
If an existing report is still valid, can it be directly cited on the application form?
You may fill in the original report number and issuing body information on the application form, but platforms may request the full original report for review, not just a citation. Additionally, you need to confirm whether the original report is still applicable to the current product, considering design changes or standard updates.
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