REACH Registration & Compliance
Navigate REACH registration with expert guidance
QbD Group helps you navigate every step of REACH registration, from substance characterization and IUCLID dossier build to SDS authoring and Chemical Safety Reporting.
What is REACH registration?
Under REACH, all chemical substances manufactured or imported into the EU/EEA in quantities of 1 tonne or more per year must be registered with ECHA.
The obligation usually applies to EU/EEA manufacturers, importers of substances or mixtures from outside the EU/EEA, and representatives acting on behalf of non-EU companies. Registration is based on the "one substance, one registration" principle and is submitted digitally via the REACH portal using IUCLID.
Why is it important?
Accurate substance identity and composition data are the foundation of a successful dossier.
Avoid duplicate testing
Proper identification helps avoid unnecessary costs and redundant studies.
Reliable hazard assessments
Accurate data ensures trustworthy risk and hazard evaluations.
Streamlined evaluation
Getting fundamentals right reduces post-submission questions and delays.
Cost efficiency
Saves time, money, and effort throughout the registration process.
How can we help?
No matter where you are in your REACH journey, we can plug in with targeted services or deliver a fully managed program.
REACH Dossier Registration
Complete dossier preparation including SIP, substance identification and analytical data package, qualitative and quantitative composition profile, impurity assessment aligned with the SIP, data gap analysis against Annex VII–XI requirements, and IUCLID data entry.
Safety Data Sheets (SDS)
REACH-compliant SDS authoring in accordance with Annex II (16 sections), including extended SDS for substances requiring exposure scenarios. Covers authoring, updates following changes in classification or hazard data, and biosafety/biosecurity assessments where relevant.
Chemical Safety Report (CSR)
End-to-end CSR support including hazard assessment (human health, physicochemical, environmental, PBT/vPvB), exposure assessment and risk characterization, CSR preparation and submission in IUCLID, and updates based on new data or regulatory changes.
Our process
We follow a structured approach to ensure your REACH registration is complete, accurate, and compliant.
1. Substance characterization
Define SIP, analytical data, and composition profile.
2. Data gap analysis
Identify missing or inadequate information against Annex VII–XI requirements.
3. Dossier preparation
IUCLID data entry, documentation upload, and CSR preparation.
4. Submission & support
Digital submission via REACH portal with ongoing compliance support.
Why QbD Group
Your trusted partner
Our team combines regulatory expertise with deep toxicological knowledge to ensure your REACH compliance.
End-to-end toxicology support
from substance characterization to dossier submission.
Trusted expertise at scale
decades of combined experience in chemical regulation.
Proactive compliance monitoring
staying ahead of REACH regulatory updates.
Certified Toxicology Experts
EUROTOX-certified (ERT) team members.
Let's talk Toxicology
From risk assessments to regulatory compliance, our toxicology experts are ready to support your pharmaceutical needs.