NaviReg
Free navigator for EU legislation
What is NaviReg?
Official texts only: All content is sourced from official EU and national authorities (e.g. EMA, EUR‑Lex, SUKL), with no content modification.
No AI or automated translation: Only official translations are uploaded. We use AI only for correctness checks.
Built by people, for people: It's a manually maintained information resource focused on being clear and easy to use.
What's inside?
Comprehensive EU regulations and guidelines: Organised by major topics like Good Pharmacovigilance Practices (GVP), GCP/GLP, cosmetics, foods for special medical purposes, and medical devices regulations.
Structured navigation:
Documents are divided into modules, chapters, sub‑chapters, and articles for readable organization.
Internal links cross‑reference between legal requirements and guidance, making the regulatory context easier to follow.
Platform status and future plans
NaviReg is currently in the phase of consultations and filling with content (the legislative requirements, guidelines, links).
As of mid‑July 2025, our NaviRegteam confirmed ongoing expansion: new regulations are continuously added and interlinked across the areas of pharmaceuticals, cosmetics, foods for special medical purposes, and medical devices.
The current design is intentionally simple: functionality and content take priority. A visual overhaul is planned for a later phase.