Testing Services | KKDIK REACH Biocidal | ISO 17025 GLP

KKDIK–REACH Similarity and Identity (UVCB, Analytical Fingerprints)

For UVCB substances or products from different suppliers, the key question is: Same substance? Incorrect identity framing leads to dossier rejection, re-testing and cost overruns. Composition/impurity comparison, analytical fingerprint (GC, LC, FTIR, NMR) and dossier-ready technical justification reports are prepared. When done correctly, data sharing and avoiding repeat tests optimise the process.

Analytical Strategy (GC/LC, FTIR, NMR, Elemental, Impurities)

Chemical identity and composition accuracy are the foundation of any dossier. GC, LC, FTIR, NMR and elemental analyses; impurity profiling and UVCB fingerprint approaches are reported in regulation-ready format. Existing reports, specifications and SDS/GBF documents are reviewed; data gaps aligned to regulation logic are then identified.

Biocidal Dossier Needs (OECD, GLP, Tox/Eco-tox, Phys-chem)

For biocidal products, formulation alone is not enough; claimed efficacy and safety are evaluated together. OECD- and GLP-compliant toxicological and ecotoxicological tests; physicochemical parameters and stability/shelf-life studies are managed. Efficacy testing, packaging compatibility and dossier-ready reporting are coordinated with laboratories.

GPSR Product Safety Testing (Risk Assessment, EN/ISO Mapping, Tech File)

Under GPSR, risk assessment, EN/ISO-compliant test plans and technical file preparation are required for general consumer products. Chemical restrictions, mechanical risks and fire/electrical safety tests are planned by target market and product class. Pier Compliance aligns the test strategy with regulatory expectations.

ISO/IEC 17025 Lab Coordination

Sample submission, acceptance criteria, method validation and report review are coordinated with ISO/IEC 17025 accredited laboratories. Results are delivered in a format consistent with SDS/GBF and registration dossiers. Alternative data strategies are evaluated where appropriate to avoid unnecessary repeat testing.

Deliverables: Test Plan, Gap Report, Dossier-Ready Evidence, Audit Pack

Test plan, data gap report, dossier-ready evidence set and audit pack are our concrete deliverables. Consistent, defensible documentation is provided for customer QA, customs, market surveillance and authority audits.

Timeline and Process Steps

Discover (scope) → Plan (test strategy) → Test (lab coordination) → Review (report verification) → File (IUCLID/dossier integration). Delivery timelines are set according to urgency.

How We Work

Share your product/substance list and existing reports; we deliver a data gap summary and a clear testing roadmap.

Current data scan
Data gap analysis (KKDIK / Turk REACH, REACH, biocidal)
Test strategy and plan
Lab coordination and process tracking
Dossier-ready report set and consistency check

Common Questions About Compliance

What tests are required for KKDIK and REACH?

Physicochemical, analytical, toxicological and ecotoxicological tests depend on tonnage, use and substance type. For UVCB and similarity cases, fingerprint analyses and read-across justification are added.

What tests are needed for biocidal products?

Efficacy tests, stability tests, toxicological/ecotoxicological data and physicochemical properties are planned per BPR and Turkish legislation.

What should the GPSR technical file include?

Risk assessment, relevant EN/ISO test reports, label and instructions, product description and manufacturer information must be in the technical file.

Is an ISO 17025 accredited lab required?

For REACH, KKDIK and BPR, GLP or ISO 17025 compliant laboratories are preferred; OECD guideline compliance is required for some endpoints.

Testing Services (KKDIK / Turk REACH, REACH & Biocidal)