ECP — European Compliance Platform European Compliance Platform

CE marking · notified body · EU authorised representative · market entry

Need CE marking, testing, or EU representation?

Submit once and receive structured offers from relevant EU compliance providers.

Free for applicants
No commission
Providers respond directly
See routes
AI guide

Do you want to sell your product in the EU but don't know where to start?

No idea which directives, tests, or documents apply to your product category.

Start with AI assistant → CB · NB

Are you ready for CE certification but unsure which body to approach?

Find the right Certification Body or Notified Body for your product scope.

Find a CB or NB → LAB

Do you need to test your product against an EU standard or directive?

Find an accredited laboratory for your specific product, standard, or regulation.

Find a laboratory → REP

Need EU, UK or Swiss representation or compliance services?

EAR, GPSR RP, PRRC, REACH OR, GDPR, DSA, VAT Fiscal, WEEE/EPR, Swiss FADP, Cosmetics RP — all 11 service types.

Find a representative → CON

Are you unsure whether your technical documentation is ready for review?

Have documents but not sure if your package will pass a compliance review.

Get a doc review →

Choose the route that matches your situation

ECP is not a directory — it is a structured path from uncertainty to action.

Each route connects your product question with the right ECP workflow.

Route 1

Do you want to sell a product in the EU, but do not know where to start?

Register as an applicant and talk to the ECP AI assistant. It helps describe your product, identify unknowns and choose the right type of specialist.

QuestionWhat product do you want to sell, and in which EU country?
ClarifyWhich documents, tests and requirements are already known?
SolutionAI route and consultant matching if needed.
ActionRegistration and first request creation.
See the process

EU Provider Network: Notified Bodies, Certification Bodies & Testing Labs

—Notified Bodies
—Certification Bodies
—Testing Labs
—EU Authorised Reps
—Regulatory Advisors

Simple process

From your first question to a submitted request

ECP is not a directory. It is a structured path from uncertainty to action.

1

Submit one structured request

Fill in your product category, market, directive, and current documentation status. Your request reaches relevant providers automatically.

2

Get relevant, comparable offers

Matched providers review your context and send tailored proposals. Compare scope, timelines, and credentials side by side.

3

Choose your partner and proceed

Pick the provider that fits. Continue the project through the platform with communication history, document exchange, and status tracking.

Request examples

What a real ECP request looks like

PulseBand Monitor

Example 1

ApexBio Instruments, Canada: EU AR for PulseBand Monitor

ApexBio Instruments, a fictional Canadian manufacturer, plans to place its PulseBand Monitor, a connected patient monitoring accessory, on the EU market and needs an EU Authorised Representative before distributor onboarding.

The applicant has draft labelling, intended use, product photos and a preliminary technical file, but is unsure whether the same provider can support MDR documentation review for the PulseBand Monitor.

ECP route: EU AR providers with MDR/IVDR scope, plus optional regulatory consultants for file readiness.

EU AR MDR Technical file
VoltGate C12

Example 2

Nordlicht Handels GmbH, Germany: EMC lab for VoltGate C12

Nordlicht Handels GmbH, a fictional German importer, wants to sell the VoltGate C12, a low-voltage smart charging controller manufactured in Taiwan, and needs EMC testing before finalising the Declaration of Conformity.

The request includes the product category, operating voltage, wireless functions, target countries and whether previous test reports exist for the VoltGate C12.

ECP route: EMC testing laboratories, with RED-capable labs included if the device has radio or wireless modules.

EMC LVD RED check
DermaTrack Patch

Example 3

VitaPatch Health, Singapore: PRRC + MDR consultant for DermaTrack Patch

VitaPatch Health, a fictional Singapore medical device startup, is preparing the DermaTrack Patch, a Class IIa wearable dermatology monitoring device, and needs a PRRC service plus MDR consulting support before approaching a Notified Body.

The team has a prototype, early risk management file and draft clinical evaluation plan, but needs help checking documentation gaps and regulatory responsibilities for the DermaTrack Patch.

ECP route: PRRC service providers, MDR consultants and, later, Notified Bodies once the documentation package is ready.

PRRC MDR consultant Class IIa

Want to test the workflow?

Submit a pilot request with your product type, target regulation and current documentation status. Applicants can test the platform free of charge during pilot launch.

Why ECP

Transparency and trust, built into the process

ECP does not just connect parties. It structures the exchange so both sides know exactly what to expect.

Provider data is sourced and verified

External Provider data is collected from public official sources. Subscribed providers on ECP are reviewed before receiving applications on the platform.

Full visibility on every application

Track who received your request, who responded, and current status. No black boxes, you always see where things stand.

Structured communication, not email chaos

All clarifications and responses happen in a threaded platform context connected to your application, not scattered across inboxes.

Ready to turn a question into a request?

CE certification typically takes 6–18 months. The earlier you start, the better your position.

Start with registration. Even if you do not know the exact route yet, ECP helps shape the request, choose the provider type and move to the next step.

Free resource

Get the CE Marking checklist

A step-by-step guide for manufacturers entering the EU market. Free after registration.