CE Certification

Ensure your product complies with European Union standards. Get CE Certified and unlock access to 30+ countries across Europe with a single mark of conformity and quality assurance.



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Everything You Need to Know

Overview of CE Certification

CE Certification is a mandatory conformity marking for products sold within the European Economic Area (EEA). It indicates that a product complies with health, safety, and environmental protection standards. At Corporate Analytica, we assist businesses in achieving CE compliance efficiently—ensuring smooth market entry across Europe.

Advantages of CE Certification

  • Legal requirement to sell in the EU and EEA
  • Boosts consumer confidence and brand credibility
  • Facilitates access to 30+ European countries
  • Improves product safety and performance standards
  • Reduces product liability risks for manufacturers

Eligibility Criteria

  • Manufacturers (EU or non-EU based)
  • EU-based importers or authorized representatives
  • Products listed under CE directives (e.g., electronics, machinery, toys, medical devices)
  • Compliance with all relevant EU directives/regulations
  • Technical documentation and Declaration of Conformity required

Documents Required

  • Technical file of the product
  • Risk assessment and safety evaluation
  • Product test reports and conformity evidence
  • Declaration of Conformity (DoC)
  • User manuals and product labeling details

CE Certification Process

  1. Step 1: Identify applicable EU directives and standards
  2. Step 2: Conduct product testing and risk analysis
  3. Step 3: Prepare the technical documentation file
  4. Step 4: Draft and sign the Declaration of Conformity
  5. Step 5: Affix the CE Mark on the product
  6. Step 6: (If required) Involve a Notified Body for third-party assessment

Why Choose Corporate Analytica?

  • End-to-end CE certification support for all industries
  • Access to accredited testing laboratories and Notified Bodies
  • In-depth technical file preparation and documentation assistance
  • Compliance guidance with EU regulations and standards
  • Fast, affordable, and globally trusted service

Post‑Certification Compliance

  • Maintain updated technical documentation for 10 years
  • Ensure ongoing compliance with changes in EU regulations
  • Respond to authority requests (market surveillance)
  • Track and document any product modifications
  • Label all packaging and instructions as per CE requirements

Penalty for Non-Compliance

  • Operating without may attract heavy fines.
  • Non-renewal of license before expiry can lead to penalties.
  • False or misleading may result in legal action.
  • Severe violations can even lead to business closure.

Frequently Asked Questions (CE Certification)

Q1. What does the CE mark stand for?

CE stands for "Conformité Européenne" meaning "European Conformity." It indicates that a product meets EU safety and quality standards.

Q2. Is CE certification mandatory for all products?

No, only products listed under EU directives (e.g., machinery, medical devices, electronics) require CE certification.

Q3. How long is CE certification valid?

There is no fixed validity. As long as the product remains unchanged and the applicable EU regulations stay the same, the certification remains valid.

Q4. Can non-European companies get CE certified?

Yes, non-EU manufacturers can obtain CE certification. However, they must appoint an EU-based Authorized Representative if selling directly in the EEA.

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