Services
One service and five things behind it
Are you placing a product on the market and unsure whether you have all the documents? Do you import into the EU and need documentation and a declaration of conformity? Or do you only want to verify that what you have is complete? Then you are in the right place.
Main service
Declaration of conformity and CE marking
We work on the certification of electrical apparatus, machinery, electronics and medical devices. We are glad to help from the start of development, where we can identify safety and other risks in advance — development then runs efficiently and focuses on what matters.
If the product is already finished and you need to issue a declaration of conformity, we prepare the technical file including the risk assessment, the identification of legal requirements and harmonised standards, arrange test reports and draft the declaration itself.
Testing
Safety testing and EMC measurement
Electrical apparatus most often calls for electromagnetic compatibility testing and electrical and mechanical safety testing. We arrange the tests, attend them and work the results into the documentation.
We have extensive experience with life-support medical devices and with the technical standards that apply to them.
Related areas
What usually goes with it
Complete documentation for the equipment: design documents, the list of harmonised standards, test reports, instructions.
Assessment of the product's risks with a description of measures and recommendations on what to change in the design.
We review your current documentation and the state of the product and propose the most efficient route. For imports we assess the supplier's documents and supply what is missing.
An audit of the product and the production process and preparation of documents for management system certification.
Risk assessment and documentation under Regulation (EU) 2023/988 for consumer products not covered by their own directive.
Declaration of conformity for packaging, technical documentation and marking under Regulation (EU) 2025/40, applicable from 12 August 2026.
How we work
Documentation should help the product, not just tick a box
We do not try to be the cheapest provider on the market. What matters to us is that the client ends up with complete documentation proving conformity and with feedback on the product — that is, with information on what would be worth changing.
We adapt lead times to the client's needs. If an inspection is underway, we treat it as a priority.
Working on a specific product?
Write a few sentences about the device — what it is, where it is sold and who manufactures it. We will come back with a proposed approach, a lead time and a price.