Chemical Regulatory Compliance (EU REACH) Services
Struggling with EU REACH compliance as a non-EU manufacturer or EU importer? Whether you need to appoint a trusted Only Representative (OR), prepare a IUCLID registration dossier, or manage complex substance data, the process is demanding and unforgiving. Mistakes in classification, data submission, or supply chain roles can cost you time, money, and EU market access.
Without a reliable OR or a clear data strategy, your compliance risks multiply. Gaps in your testing data, unclear substance identity, or incomplete dossiers can trigger ECHA scrutiny, delays in registration, or even rejection of your submission. These risks are especially high for companies relying on outdated data, unclear roles, or consultants without REACH experience.
RegSurance gives you complete control over your EU REACH obligations. We offer end-to-end OR services, prepare and submit robust REACH registration dossiers, and perform data gap analysis to identify exactly what testing or waivers you need—minimising cost while ensuring full compliance. With RegSurance, you get clarity, efficiency, and confidence at every step of the REACH process.
Why Choose Our Services
Market Access Secured
We manage the entire REACH registration process to ensure your continued access to EU and UK markets—avoiding delays, rejections, or regulatory disruption.
Audit-Ready Documentation
Our REACH dossiers are technically robust, fully traceable, and prepared to meet ECHA scrutiny—so you’re always inspection-ready.
Lower Testing Costs
Through expert data gap analysis, we help you minimise animal testing and avoid unnecessary studies—saving time and cost while meeting REACH requirements.
- Authorised representative services for India Chemical Safety Management Rule
- Only representative services for EU, UK, and Turkey
- Inventory listing check
- Data requirement, waivings and gap analysis
- Performing, monitoring and coordination of studies with GLP certified laboratory partners
- Review and interpretation of testing reports
- Authoring IUCLID dossiers and other authority approved dossier formats
- Submission of dossier to authority
- Follow ups and post approval activities