CE Certification: Your Gateway to the European Market

Obtaining the CE mark demonstrates that your product complies with EU health, safety, and environmental protection standards—mandatory for lawful distribution across the European Economic Area (EEA).

The CE mark, or Conformité Européenne, acts as a passport allowing free movement of goods within the EEA and signifies conformity with all applicable EU directives and regulations.

Partner with DoStartup™ to streamline the CE certification process and confidently enter one of the world’s most robust and business-friendly markets.

Overview Illustration

Registration Form

Let our CA-certified experts handle your business registrations , legal compliance, and tax needs — while you focus on growing your business with peace of mind.

What You Get:

  • Personalized Expert Guidance
  • Hassle-Free Documentation
  • Fast & Transparent Process
  • Dedicated Support Team
  • Affordable & Flexible Plans
  • Secure & Confidential Handling
  • Timely Updates & Reminders
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Free Consultation by Expert

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Features That Empower You

We provide end-to-end solutions with expert support, ensuring your journey is seamless and stress-free.

Legal Market Access

CE marking is a legal requirement for many regulated products to enter and circulate freely within the EEA.

Harmonized Standards

Ensures all manufacturers adhere to the same EU directives for health, safety, and environmental protection.

Conformity Assessment

Supports both self-assessment for low-risk products and notified body evaluation where required.

Consumer Safety

Protects end users by mandating rigorous testing and risk assessment before market entry.

Free Movement of Goods

Eliminates country-specific approvals—once CE marked, products can be sold across the entire EEA.

Who Needs to Register?

Fair Competition

Level playing field ensuring all products meet the same mandatory EU requirements.

Market Confidence

Enhances product credibility and consumer trust through demonstrated compliance.

Regulatory Protection

CE mark holders gain legal protection from enforcement actions when correctly certified.

Global Recognition

Widely respected outside Europe as a mark of high regulatory compliance.

How To File It Online?

Follow this step-by-step guide to ensure your response is submitted correctly

Form Fill
1

Identify Applicable Directives

Determine which EU directives and harmonized standards apply to your product.

2

Conformity Assessment

Choose self-assessment or engage a notified body based on product risk classification.

3

Compile Technical File

Assemble product specifications, test reports, risk assessments, and design documentation.

4

Draft EU Declaration of Conformity

Formalize compliance in a signed declaration, referencing all applicable directives.

5

Affix CE Mark

Place the CE logo (minimum 5 mm height) and notified body number (if any) on the product or packaging.

Deadlines & Penalties

Avoid late fees by submitting on time

Penalty for Late Filing

  • Product description and technical specifications
  • Test reports verifying compliance with EU harmonized standards
  • Risk assessment documentation
  • Signed EU Declaration of Conformity
  • Notified body certificate number (if applicable)

Consequences of Non-Compliance

  • Market withdrawal or bans for non-compliant products
  • Fines or legal action by EU authorities
  • Damage to brand reputation and customer trust

1Who Needs CE Certification?

  • Manufacturers, importers, or distributors of products covered by EU directives
  • Products in categories such as medical devices, toys, PPE, electronics, machinery, and more
  • Low‑risk products may self‑certify; higher‑risk items require notified body involvement

2Key Technical Requirements

  • Compliance with all relevant EU directives and harmonized standards
  • Maintenance of a complete technical file for at least 10 years post‑market placement
  • Signed EU Declaration of Conformity kept up to date

3Products Eligible for CE Certification

  • Electrical and Electronic Equipment
  • Medical Devices
  • Toys and Children’s Products
  • Household Refrigerators and Freezers
  • Personal Protective Equipment (PPE)
  • Radio and Telecommunications Equipment
  • Gas‑Fired Hot‑Water Boilers
  • Lifts and Elevators
  • Measuring Instruments
  • Pressure Equipment and Simple Pressure Vessels

4Checklist to Obtain CE Marking

  • Identify applicable EU directives and regulations
  • Determine appropriate conformity assessment procedure
  • Prepare and maintain a comprehensive technical file
  • Conduct product testing (in‑house or third‑party)
  • Draft and sign the EU Declaration of Conformity
  • Affix CE marking and notified body number (if required)
  • Retain Declaration of Conformity and technical file for 10 years
  • Self‑verify low‑risk products when third‑party testing is not mandatory
AspectISO CertificationCE Certification
PurposeQuality and process standardsProduct compliance with EU directives
ScopeOrganizations across all sectorsProducts sold in the EEA
AssessmentExternal audit by certification bodySelf‑declaration or notified body assessment
Voluntary vs MandatoryVoluntaryMandatory for regulated product categories

Why Trust DoStartup?

Professional services with guaranteed satisfaction

Directive & Standard Mapping

Identify all applicable EU directives and harmonized standards for your product category.

Technical File Assembly

Compile and review product specifications, test reports, risk assessments, and manuals.

Notified Body Coordination

Liaise with EU‑recognized notified bodies for required third‑party assessments.

Declaration Drafting

Prepare a precise EU Declaration of Conformity signed by authorized representatives.

Marking & Labeling Guidance

Ensure CE logo and notified body numbers are correctly sized, proportioned, and placed.

Frequently Asked Questions

Have a look at the answers to the most asked questions

What is CE Certification?

Is CE Certification valid in India?

Is CE Marking accepted in the United States?

Who issues CE Certification?

When is CE Certification mandatory in Europe?

What is the difference between ISO and CE Certification?

Do medical devices require CE marking?

Is CE marking required for machinery?

What is minimal risk in CE Certification?

What is a Declaration of Conformity?

How do you affix the CE mark?

Does CE Certification expire?

How long must I keep the technical file?

When is an independent assessment needed?

How do I find a Notified Body?