EU REACH + UK REACH + emerging-jurisdiction chemical regulation across the full substance lifecycle
EU REACH (1907/2006, in force since 2007) remains the world's most rigorous chemical regulation, now joined by UK REACH (post-Brexit, with parallel registration deadlines extending to 2030 under ATR3), Switzerland's CH-REACH, Turkey's KKDIK, China's MEE Order 12 (new chemical substance notification), Korea's K-REACH, and emerging Asian equivalents in Taiwan (TCSCA), Japan (CSCL), Vietnam, and Indonesia. The 2024 EU CSS (Chemicals Strategy for Sustainability) revision tightens the Authorisation List, expands Restriction (Annex XVII) entries, and introduces generic risk assessment under the new One Substance One Assessment (OSOA) framework. Modern REACH practice now also navigates ECHA REACH-IT and IUCLID 6.x dossier preparation, OR (Only Representative) appointment strategy for non-EU manufacturers, SVHC tracking (now 240+ substances), exposure scenario development for CSR Annex authoring, and downstream-user obligations under Article 37 / 38. The PFAS Restriction (proposed 2023, expected adoption 2026–2027) represents the largest single restriction in REACH history and will affect 10,000+ substances and millions of articles.

A practical, phased delivery approach — from gap assessment through operational embedding — built around your regulatory context.
Build substance inventory per CAS / EC / IUPAC; identify REACH applicability (>1 tonne/year EU import / manufacture); conduct pre-registration via ECHA REACH-IT; align with EU REACH Regulation 1907/2006 phase-in / non-phase-in deadlines.
Generate data per tonnage tier — Annex VII (>1 t), VIII (>10 t), IX (>100 t), X (>1000 t); apply alternative methods (read-across, QSAR, in-vitro) per OECD validated methods; align with ECHA testing proposal requirement.
Conduct CSA per Annex I for substances >10 t/y — hazard assessment, PBT / vPvB assessment, exposure assessment per use descriptor, risk characterisation; document in Chemical Safety Report (CSR) via ECHA IUCLID / Chesar.
Compile registration dossier in IUCLID 6 — substance identification, classification, study summaries, exposure scenarios, downstream use; submit to ECHA via REACH-IT; align with joint submission (lead registrant + co-registrants).
Track Substance of Very High Concern (SVHC) Candidate List, Authorisation List (Annex XIV), Restriction List (Annex XVII); design substitution programme per ECHA Substitute It Now; align with corporate product stewardship.
Manage downstream user obligations — Article 32 SDS communication, Article 37 use notification, Article 38 reporting; maintain dossier updates per Article 22 trigger events; align with REACH compliance auditing per ECHA enforcement programme.

Speak with our team to scope an engagement tailored to your facility, regulatory context, and lifecycle stage.