ECP — European Compliance Platform European Compliance Platform
EU Compliance Marketplace

The EU Compliance Marketplace

ECP is the neutral EU compliance marketplace for Notified Bodies, Certification Bodies and testing laboratories. Non-EU manufacturers submit one structured request and receive proposals from matched providers across all major EU regulations. EU representation and regulatory consulting are offered separately by AFINA s.r.o., the company behind ECP.

How it works →

What is an EU compliance marketplace?

An EU compliance marketplace is a platform where non-EU manufacturers submit structured compliance requests and receive proposals from matched providers. On ECP, these are Notified Bodies, Certification Bodies and testing laboratories. Unlike working with a single consultancy, you can compare scope, timeline and pricing across several providers before committing. For these categories ECP is neutral: it does not sell conformity assessment, certification or testing itself.

A marketplace lets you compare several providers instead of relying on one firm’s recommendation. ECP does not sell conformity assessment, certification or testing; it gives you access to those who do. EU representation and regulatory consulting are offered separately by AFINA s.r.o., the company behind ECP.

EU compliance service categories on ECP

CategoryWhat it coversFind a provider
Notified Body (NB) MDR Class IIa–III conformity assessment, IVDR Class B–D Find a Notified Body
Testing Laboratory EMC testing, RED (radio), safety testing for CE marking Find a Testing Lab
Certification Body (CB) ISO 13485, MDSAP, product certification Find a CB

EU representation and regulatory consulting are offered separately by AFINA s.r.o., the company behind ECP. View AFINA services

Why choose a marketplace over a single consultancy?

FactorSingle consultancyECP marketplace
ObjectivityRecommends their own servicesNeutral for NB, CB and lab matching
ChoiceOne providerMultiple proposals, you decide
Price transparencyOpaque — no benchmarkCompare real quotes side-by-side
CoverageLimited to their expertiseNetwork covers all EU regulations
TimeSequential outreachOne request → multiple responses

How ECP works

  1. Submit a structured request — describe your device or product category, applicable regulation, target EU markets, and compliance need. Takes approximately 5 minutes.
  2. ECP routes your request — we match it to relevant providers in the network based on designation scope, product category, regulatory expertise, and current availability.
  3. Receive proposals — providers respond directly with their scope, timeline, and pricing. You review, compare, and decide with no obligation.

See the full route for your regulation

RegulationWhat the ECP route looks like
MDRECP for MDR — testing lab and Notified Body →
GPSRECP for GPSR — confirm it applies, appoint your RP →
RED / EMC / LVD / Machinery / PPEECP for CE Marking — testing and NB where required →

Regulations covered by ECP

  • MDR 2017/745 — Medical Devices Regulation
  • IVDR 2017/746 — In Vitro Diagnostic Regulation
  • RED 2014/53/EU — Radio Equipment Directive
  • EMC Directive 2014/30/EU — Electromagnetic Compatibility
  • LVD — Low Voltage Directive 2014/35/EU
  • Machinery Regulation (EU) 2023/1230
  • GPSR Regulation (EU) 2023/988 — General Product Safety Regulation
  • EU Cosmetics Regulation 1223/2009
  • PPE Regulation (EU) 2016/425 — Personal Protective Equipment

What is an EU compliance marketplace?

An EU compliance marketplace is a platform where non-EU manufacturers submit structured compliance requests and receive proposals from matched providers. On ECP, these are Notified Bodies, Certification Bodies and testing laboratories. Unlike working with a single consultancy, you can compare scope, timeline and pricing across several providers before committing.

What is the difference between ECP and a regulatory consultancy?

A regulatory consultancy sells its own services and naturally recommends its own approach. For Notified Bodies, Certification Bodies and testing laboratories, ECP is a neutral marketplace: it does not sell those services itself, so its only incentive is to match you with the provider that best fits your device, risk class and timeline. EU representation and regulatory consulting are different: they are offered by AFINA s.r.o., the company behind ECP, and we say so openly.

Which EU compliance services does ECP cover?

ECP matches three provider categories: Notified Bodies (MDR and IVDR conformity assessment), Certification Bodies (ISO 13485, MDSAP, product certification) and testing laboratories (EMC, RED, safety testing). EU representation (EC REP, GPSR and cosmetics Responsible Person, REACH OR, PRRC) and regulatory consulting are not matched on ECP; they are offered directly by AFINA s.r.o., the company behind ECP.

Is ECP free to use?

Search is free and unlimited for applicants — no account needed. Your first project is free to send to a small set of matched providers; sending to more, or a further project, uses a one-time package — no subscription. Service providers currently join and respond free during ECP's Early Access phase; a paid provider subscription may be introduced later.

Representative & compliance roles

Non-EU manufacturers and businesses entering EU, UK and Swiss markets often also need one of the representative or compliance roles below. These roles are not part of ECP’s provider matching: EU representation and regulatory consulting are offered separately by AFINA s.r.o., the company behind ECP, some of them together with partner firms. The linked pages explain each role.

ServiceDescriptionRegulationMore
EU Authorized Representative (EAR) Mandatory EU-based representative for non-EU manufacturers placing regulated products on the EU market. MDR / IVDR / RED / LVD Find EC REP
UK Representative (UK RP) UK-based Responsible Person for non-UK manufacturers placing UKCA-marked products on the GB market. UK MDR 2002 / UKCA Find UK RP
PRRC Services Person Responsible for Regulatory Compliance (Art. 15) for medical device manufacturers without in-house PRRC. MDR / IVDR Art. 15 Find PRRC
GPSR Responsible Person EU-based Responsible Person for general consumer products sold in the EU, including online marketplaces. GPSR 2023/988 Find GPSR RP
EU Cosmetics Responsible Person Responsible Person for non-EU cosmetics brands including CPNP notification and PIF management. Cosmetics Regulation 1223/2009 Find Cosmetics RP
GDPR Article 27 Representative EU data protection representative for organisations outside the EU processing personal data of EU residents. GDPR (EU) 2016/679 Art. 27 Find GDPR Rep
DSA Article 13 Legal Representative EU legal representative for digital service providers established outside the EU serving EU users. DSA (EU) 2022/2065 Art. 13 Find DSA Rep
REACH Only Representative EU representative for non-EU chemical substance manufacturers managing ECHA registration and SDS obligations. REACH (EC) 1907/2006 Find REACH OR
VAT Fiscal Representative EU VAT registration and fiscal compliance for non-EU businesses selling in EU member states. EU VAT Directive 2006/112/EC Find VAT Rep
WEEE / EPR Compliance Registration in national WEEE registries and take-back compliance for electronics and packaging producers. WEEE 2012/19/EU / EPR schemes Find WEEE/EPR Provider
Swiss FADP Representative Swiss data protection representative for organisations outside Switzerland processing Swiss residents’ data. Swiss FADP / nDSG Art. 14 Find Swiss FADP Rep

For representation, see AFINA services — operated by AFINA s.r.o., the company behind ECP, and distinct from ECP’s independent LAB, CB and NB provider matching.

Submit your first compliance request

Describe your device or product and receive proposals from matched Notified Bodies, Certification Bodies and testing laboratories. Search is free — your first project is free to send; further projects use a one-time package, no subscription.

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