CE Mark Testing
The Latest International Standards & Specifications
GME is an ISO 17025 accredited laboratory testing products for compliance with the European Union Directives. We use the latest international EMC/electrical-safety standards and electronics specifications.
The EMC laboratory is equipped with the essential conducted emissions, electrostatic-discharge and magnetic immunity capabilities. Conducted disturbance testing includes electrical fast transients, surges, radio-frequency noise, and voltage variations. Radiated emissions testing is done on the Open Area Test Site, and radiated-immunity tests are performed in the anechoic shielded chamber.
Product safety measurement capabilities include electric strength, leakage current, insulation resistance, and ground bond. Environmental test capabilities include dry heat to 175ºC, humidity to 99%, and cold to -40ºC.
CE Testing Can Be Performed on Equipment in The Following Groups:
- Commercial
- Residential
- Light-industrial
- Industrial
- Scientific
- Medical (ISM)
- Information-technology (ITE)
- Measurement
- Control
- Laboratory
- Marine
- Automatic identification systems (AIS)
- Short-range-devices
- and more…
Basic Steps to Putting the CE Mark on Products to Be Shipped Into the EU:
Decide Which Directives Apply to Your Export Product
- Electromagnetic Compatibility
- Electrical (Low-Voltage) Safety
- Machinery Safety
- Medical Devices
- Radio Equipment
The equipment manufacturer identifies the proper directives that apply to a product. For example, if the product is equipped with moving parts, the machinery safety standard will apply.
Determine Which Standards Apply and Perform Tests
After choosing the directives that apply, a manufacturer then selects the applicable harmonized (EN) product standards and performs the required tests. The International Electrotechnical Commission (IEC) writes many EN standards. GME is available to answer questions about standards, as well as perform tests.
Declaration of Conformity
When a product is tested and determined to be in compliance with applicable standards, a Declaration of Conformity (DoC) is created in accordance with ISO/IEC 17050-1/2. Reports generated by the test lab, as well as design documentation, act as “supporting documentation” in validating the DoC. Test records, drawings, risk analysis, etc., and the DoC are held on file and made available at any time for review by “competent authorities”. A copy of the DoC should be submitted to your distributor, representative, or importer in the EC. It is also good practice to include a copy of your DoC in your instruction manual.
Sample Declaration of Conformity (DoC)
CE Mark
To show proof of conformity, the EU makes it mandatory for the manufacturer to label the product with the CE mark. The label, “CE”, must be attached in an indelible manner, look like the CE in the EU artwork, and be no less than 5-mm in dimension. Whether reduced or enlarged the proportions given above must be maintained. The marking should be affixed to the product, or if this is not possible, to the packaging, instructions for use, or warranty certificate.
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You can also reach us directly at gme@gmelectro.com or 802-388-3390.
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Frequently Asked Questions
CE testing verifies that a product meets European Union directives and regulations and is suitable for application of the CE-Mark. EU directives and regulations include electrical safety (Low-Voltage Directive), electromagnetic compatibility (EMC Directive), machinery (Machinery Regulation) and wireless devices (Radio Equipment Directive). Products to be sold in the EU must comply with the appropriate EN standards (European Norms) which show they meet the applicable directives and regulations before they can legally bear the CE Mark and enter the European market.
The path to the CE-Mark for most products is the CE Manufacturer’s Declaration of Conformity (CE DoC) process in which an ISO 17025 accredited laboratory, such as GME, tests the product for compliance with the applicable EN standards and issues compliant reports to the manufacturer. The manufacturer then issues the CE DoC based on successful test results, applies the CE-Mark to the product, and ships it to the EU. This streamlined process applies to items such as measurement, control and laboratory equipment. Multimedia equipment, machines and devices incorporating CE approved radio modules can also use this path.
A small number of products, such as new radio designs and dangerous equipment, cannot use the CE DoC process and manufacturers must have their product tested and certified by an EU Notified Body.
Timelines depend on product complexity, applicable standards, and design readiness.
Typical project durations range from:
1–2 weeks for straightforward EMC and Safety testing
3–6+ weeks for complex or multi-standard compliance projects including Cybersecurity
Costs vary depending on:
Applicable standards and directives
Product complexity
Required test scope
Number of configurations
Need for pre-compliance testing
We provide clear, project-based quotations after reviewing your product specifications and intended markets. That being said, projects can range on average between $3,000 - $10,000.
EMC testing is required for most electronic and electrical products, including:
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Consumer electronics
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Industrial equipment and machinery
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Medical devices
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Automotive electronics
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Wireless and IoT devices
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Laboratory and scientific equipment
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Measurement and control equipment
If your product contains switching electronics, digital circuitry, wireless modules, or power conversion components, EMC compliance is typically required.
Yes. GME has decades of experience helping manufacturers meet standards. Design iteration and troubleshooting are common parts of the compliance process. We work closely with engineering teams to identify root causes of non-compliance and recommend corrective actions to help you pass testing efficiently.
CE Marking is used to show that a product complies with applicable EU directives and regulations. Depending on the product, this can require EMC, Safety & Cybersecurity testing, inspection and technical documentation.
FCC Certification by a Telecommunication Certification Body (TCB) is a formal authorization process only required for electronic devices that emit RF energy intentionally. A TCB will assign an FCCID to a certified product before it is marketed or sold in the U.S.
If you plan to sell your product in both the European Union and the United States, you will likely require both CE and FCC compliance. Each market has its own regulatory framework and testing requirements which GME will be happy to help you navigate.
A non-CE compliant product cannot be shipped to the EU. If a product cannot demonstrate conformity with applicable EU directives, it may be detained or denied entry at EU customs. Authorities will review your CE DoC and can request your Technical Documentation to verify compliance.
If non-compliance is identified — either at import or through market surveillance — consequences may include shipment holds, product recalls, fines, or removal from the EU market.
GME helps manufacturers avoid this situation with thorough structured testing and complete technical documentation support.