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Certification services grouped by technology
Compliance FAQ
Real questions buyers ask before export — each routes to a standard explainer, a market compliance path, or the Compliance Checker.
New Product Launch
- QWhat certification does a wireless product need for the EU?
- View market compliance path
- QWhat is the difference between FCC and UL certification in the US?
- View market compliance path
- QWhich tests are covered by the CE RED directive?
- View standard details
- QDoes toy export to the EU require EN 71?
- View standard details
- QDoes a car product exported to the EU need eCall?
- Use Compliance Checker
- QWhat do Japan PSE and TELEC each regulate?
- View market compliance path
- QDoes a Bluetooth product need BQB certification?
- Use Compliance Checker
- QWhat standards govern EMC testing?
- View standard details
- QWhich substances are restricted by RoHS for electronics?
- View standard details
- QWhat is the difference between FCC ID and SDoC?
- View standard details
- QWhich certifications does a smart speaker export require?
- Use Compliance Checker
- QWhat does a new-energy battery export to the EU require?
- View market compliance path
- QWhich tests does automotive export to the US require?
- View market compliance path
- QDoes toy export to the US require ASTM F963 and CPSIA?
- Use Compliance Checker
- QWhat is Article 3.2 testing under EU RED 2014/53/EU?
- View standard details
- QDoes a Bluetooth headset need EN 300 328 for the EU?
- View standard details
- QDoes a product with lithium batteries need UN 38.3 for the EU?
- View standard details
- QWhich standards are covered by the EU EMC Directive 2014/30/EU?
- View standard details
- QWhat is the difference between FCC Part 15B and Part 15C?
- View standard details
- QHow is Japan TELEC (Giteki) certification done for wireless products?
- View standard details
- QDoes Japan PSE certification have diamond and round categories?
- View standard details
- QDoes an in-vehicle infotainment system need eCall for the EU?
- Use Compliance Checker
- QDoes automotive electronics export to the US need FCC or ISED?
- View market compliance path
- QWhat certifications does a smartwatch need for the EU?
- View market compliance path
- QDoes a smart home gateway need FCC ID for the US?
- View market compliance path
- QDoes a power tool need EN IEC 62841 for the EU?
- Use Compliance Checker
- QDoes a medical device need EU MDR and electrical safety for the EU?
- Use Compliance Checker
- QBesides UN 38.3, does lithium battery shipping need an MSDS?
- View standard details
- QWhich substances does EU RoHS 2.0 restrict?
- View standard details
- QHow to address EU REACH SVHC for electronics?
- Use Compliance Checker
- QDoes a wireless charger need Qi and RED for the EU?
- View standard details
- QDoes a power adapter for the EU need EN 62368-1?
- View standard details
- QDoes children's audio need EN 71 and EN 50332 for the EU?
- View standard details
- QAre US UL 62368-1 and FCC mandatory?
- Use Compliance Checker
- QWhat is the impact of the EU common charger directive on phones?
- View standard details
- QDoes a speaker need TELEC and PSE for Japan?
- View market compliance path
- QWhat are EU IoT cybersecurity requirements (RED DA) for exports?
- View standard details
General Compliance
- QWhat test is required to ship lithium batteries by air?
- View standard details
- QIs the laboratory CNAS accredited?
- View answer & next step
- QHow long does a test report usually take?
- Use Compliance Checker
- QHow can I verify your testing capabilities?
- View answer & next step
- QAre your test reports internationally recognized?
- View answer & next step
New Market Entry
- QDo I need SABER to export to Saudi Arabia?
- View answer & next step
- QWhat is the minimum compliance path to enter the US market?
- View answer & next step
- QDoes a wireless product need UKCA to enter the UK?
- View answer & next step
- QHow does multi-country certificate transition work?
- View answer & next step
- QCan you handle CB certification?
- View answer & next step
- QDo electronic consumer goods need UKCA or CE for the UK?
- View answer & next step
- QWhat are the requirements for home appliances entering Saudi Arabia?
- View answer & next step
- QWhich electronics does India BIS certification apply to?
- View answer & next step
- QHow is the Australia RCM mark applied for?
- View answer & next step
- QDoes Korea KC certification cover wireless products?
- View answer & next step
- QWhat are Brazil ANATEL requirements for wireless products?
- View answer & next step
- QWhat is the difference between Canada ISED and FCC?
- View answer & next step
- QWhich products does China CCC certification cover?
- View answer & next step
- QHow to do multi-country certification most cost-effectively?
- View answer & next step
Certificate Renewal
- QHow to renew or transition an expired certificate?
- View answer & next step
- QCan a lost certificate be reissued?
- View answer & next step
Platform & Customs Inquiry
- QHow to respond to an Amazon compliance inquiry?
- View answer & next step
- QWhat compliance documents does customs inspection require?
- View answer & next step
Technical Q&A
The quantity is driven by the test scope, not by the product category. A single EMC plus safety series for a consumer device is normally built around two to three production-representative units, while battery testing can consume several dozen cells because T.1-T.8 includes destructive tests.
What matters more than the count is the condition. Samples must match the final production build, carry the final firmware, and be shipped with the accessories and packaging that will actually be sold. Any deviation has to be declared, because the report is valid only for the configuration that was tested.
The exact quantity is fixed in the test plan and quotation before you ship, so you are not guessing.
What matters more than the count is the condition. Samples must match the final production build, carry the final firmware, and be shipped with the accessories and packaging that will actually be sold. Any deviation has to be declared, because the report is valid only for the configuration that was tested.
The exact quantity is fixed in the test plan and quotation before you ship, so you are not guessing.
Yes, and it is usually the cheaper route. Bring the lab in at EVT, when the enclosure, the grounding scheme and the antenna layout can still change. A pre-compliance sweep at that stage tells you whether the design will survive formal testing while fixes are still a board revision rather than a tooling change.
By DVT the design should be close enough to run the formal series. By MP, testing can only confirm what has already been built, and a failure at that point means tooling and inventory.
If the schedule leaves no room for a pre-test, at least send the critical configuration for a single EMC scan.
By DVT the design should be close enough to run the formal series. By MP, testing can only confirm what has already been built, and a failure at that point means tooling and inventory.
If the schedule leaves no room for a pre-test, at least send the critical configuration for a single EMC scan.
A failed item is not a failed project. The report records the measured value against the limit, and our engineers review the setup with you to separate a design issue from a test-configuration issue - a cable routed differently or an accessory left attached can produce a failure that has nothing to do with the product.
Retesting is normally limited to the failed items rather than the full series, and it is quoted separately because the scope differs each time. The product has to come back as a new sample that reflects the fix; a unit modified on the bench cannot be passed without being verified again.
Most fixes sit in grounding, filtering, cable routing or firmware power settings.
Retesting is normally limited to the failed items rather than the full series, and it is quoted separately because the scope differs each time. The product has to come back as a new sample that reflects the fix; a unit modified on the bench cannot be passed without being verified again.
Most fixes sit in grounding, filtering, cable routing or firmware power settings.
Pre-compliance is our own engineering scan. The methods are the same but the result is not a formal, traceable conclusion - its purpose is to find problems while they are still cheap to fix. Formal certification testing is performed to the full standard, with calibrated equipment and documented uncertainty, and produces a report that a Notified Body, a marketplace or a customs officer will accept.
Running the first before the second is what keeps a project on schedule. A pre-scan typically adds a few days and removes the most common cause of a four-week delay.
Running the first before the second is what keeps a project on schedule. A pre-scan typically adds a few days and removes the most common cause of a four-week delay.
No, and buyers frequently ask for the wrong one. A test report is issued by the laboratory: it states what was tested, how, and the measured results against the limit. A certificate is issued by a certification body or an authority and carries a registration number that can be verified independently.
For most CE directives there is no such document as a 'CE certificate'. Conformity is demonstrated by the technical file, the test reports inside it, and a Declaration of Conformity signed by the manufacturer. A certificate is genuinely mandatory for access schemes such as TELEC, KC, BIS or CCC, where the authority issues the approval itself.
For most CE directives there is no such document as a 'CE certificate'. Conformity is demonstrated by the technical file, the test reports inside it, and a Declaration of Conformity signed by the manufacturer. A certificate is genuinely mandatory for access schemes such as TELEC, KC, BIS or CCC, where the authority issues the approval itself.
The technical file is legally the manufacturer's responsibility, but we routinely compile the test-related sections on the client's behalf. A file that survives scrutiny contains: product description and intended use, rated specifications, an illustrated build description, block diagram and schematics, bill of materials, certificates for safety-critical components, the risk assessment, the test reports, the user manual in the language of the target market, and the signed Declaration of Conformity.
It has to be kept for ten years after the last unit is placed on the market and be handed over on request. The usual failure is not a missing file but a missing risk assessment or manual translation.
It has to be kept for ten years after the last unit is placed on the market and be handed over on request. The usual failure is not a missing file but a missing risk assessment or manual translation.
Formal testing is not a best-case demonstration. The worst-case configuration is the build and operating mode that produces the highest emission or the lowest immunity margin, and identifying it is engineering work rather than a formality.
In practice it usually lands on the variant with the fastest clock, the highest output power, the longest cable, the densest packing, or the firmware mode that stresses the radio hardest. When a family covers several models, we normally test the worst case and document the engineering rationale that ties the other models to it - that rationale is what makes a family approval defensible in front of an authority.
In practice it usually lands on the variant with the fastest clock, the highest output power, the longest cable, the densest packing, or the firmware mode that stresses the radio hardest. When a family covers several models, we normally test the worst case and document the engineering rationale that ties the other models to it - that rationale is what makes a family approval defensible in front of an authority.
A quotation should let you see the boundary of the work. Ours is built from four lines: engineering and test time per standard, report preparation, the certification body fee where a certificate is required, and any witnessed testing or travel.
What is charged separately is almost always reactive: retests after a failure, additional samples, extra configurations, translation of manuals, and Notified Body review or annual surveillance fees - those are set by the body, not by us. Ask for those lines explicitly before you approve a purchase order. A quotation that looks cheapest very often excludes exactly them.
What is charged separately is almost always reactive: retests after a failure, additional samples, extra configurations, translation of manuals, and Notified Body review or annual surveillance fees - those are set by the body, not by us. Ask for those lines explicitly before you approve a purchase order. A quotation that looks cheapest very often excludes exactly them.
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