ECP European Compliance Platform

Normative requirements (EU/CE)

A practical orientation for applicants: official sources, CE workflow, and key EU acts by product area. We provide links only (no copies). Always verify the latest consolidated version and applicability dates on EUR-Lex.

Disclaimer: This page is for navigation and does not constitute legal advice. Harmonised standards are often paid documents; use official catalogues to check versions.

Start here (official sources)

CE workflow (high level)

  • Identify all applicable EU legislation for your product (often more than one).
  • Determine the conformity assessment route (self-declaration vs Notified Body).
  • Compile technical documentation, risk assessment, test evidence, instructions & labelling.
  • Issue the EU Declaration of Conformity and affix CE marking (where applicable).

Harmonised standards: where to check lists & versions

Harmonised standards provide "presumption of conformity" when correctly applied. Always check the Official Journal references (OJEU) and the latest citations for your legislation.

Key EU acts by product area (quick map)

Tip: open each section to see typical legislation and official links. Some areas have additional requirements (chemicals, batteries, ecodesign, packaging, etc.).

Electrical / Electronics
Machinery / Industrial equipment
Personal Protective Equipment (PPE)
Medical devices / IVD
Toys
Construction products
Gas appliances
Lifts
Measuring instruments / scales
Horizontal rules (often relevant)

What applicants typically need to prepare

  • Product description & intended use (scope).
  • Bill of materials / critical components (where applicable).
  • Risk assessment (especially machinery, PPE, medical).
  • Test reports (or test plan) against relevant standards.
  • Instructions, labels, and traceability info (manufacturer/importer).
  • Draft EU Declaration of Conformity (when applicable).