CE Mark
CE marking support that maps the exact directive your product falls under.
We help identify which EU directive(s) and standards apply to your product, organise the technical file, and coordinate with a notified body where third-party assessment is required.
What is CE Mark?
CE marking indicates that a product meets applicable European Union health, safety and environmental protection requirements, and is a legal requirement for placing many product categories on the market in the European Economic Area — not a voluntary quality certification.
Depending on the product category (machinery, electronics, medical devices, PPE, toys and others), the manufacturer either self-declares conformity after preparing the required technical file, or must involve an EU-recognised 'notified body' for independent assessment.
Gurur Consultancy helps identify the correct EU directive(s) and harmonised standards for your product, organise the technical documentation, and coordinate with the appropriate notified body where third-party assessment is required — we do not issue CE marking ourselves, and only the manufacturer can affix it once conformity is established.
Why this matters for your business
Who typically needs CE Mark?
Applicability varies by business — here’s who this usually applies to.
- Manufacturers and exporters of machinery, electrical/electronic equipment
- Medical device and PPE manufacturers targeting EU markets
- Toy, construction product and other manufacturers in CE-regulated categories
Eligibility & requirements
- Applies specifically to product categories covered under EU CE-marking directives — not every product requires it
- Requirements and assessment routes (self-declaration vs. notified-body involvement) vary by product category
Documents & information
Commonly required documents may include:
How we take this forward
- 01
Directive Identification
We help identify which EU directive(s) and harmonised standards apply to your specific product.
- 02
Risk Assessment
A risk assessment is conducted for the product category, as the directives require.
- 03
Technical File Preparation
We help compile the technical documentation, test reports and declarations required.
- 04
Testing / Notified Body Coordination
Where third-party assessment is required, we coordinate testing and submission to an EU-recognised notified body.
- 05
Declaration of Conformity
The manufacturer issues a Declaration of Conformity once all requirements are met.
- 06
CE Marking Applied
The manufacturer affixes the CE mark to the product, as the applicable directive permits.
Our approach to CE Mark
End-to-End Support
One partner from idea to registration to tender win.
Practical Guidance
Plain-language advice from people who have filed thousands of cases.
Documentation Support
Right documents, right format, right the first time.
Compliance-Focused Approach
We don't just register — we keep you compliant.
Government Procurement Expertise
We know GeM, CPP and tender portals inside-out.
Long-Term Business Support
We grow with you — from proprietorship to private limited.
Frequently asked questions
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Need Help With CE Mark?
Tell us about your product and target EU market, and we'll help identify the applicable CE requirements.