GLP stands for Good Laboratory Practice—a set of internationally recognized quality standards that ensure the reliability and integrity of non-clinical laboratory studies. GLP-compliant studies are often required by regulatory authorities (e.g., under REACH or BPR) for chemical registration or product approvals.

No. We do not operate a testing laboratory ourselves. Instead, we specialize in developing GLP-compliant testing strategies and coordinating studies through trusted, certified laboratory partners. This approach ensures you get high-quality results without managing the process alone.

The exact studies depend on your product type, intended use, and applicable regulations. These can include toxicological studies (e.g., acute toxicity, skin irritation), ecotoxicological tests (e.g., algae growth inhibition), or physical-chemical testing (e.g., partition coefficient). We help you identify which ones are needed and why.

We only work with GLP-certified laboratories and design your testing program based on current regulatory requirements. We also review study plans and reports to ensure they meet the standards expected by authorities—helping you avoid delays or rejections.

Yes. Whether you are mid-project or need support reviewing a draft report, we can step in at any stage to ensure your study is on track, compliant, and well-documented for submission.

Timelines vary depending on the type and complexity of the study. Some basic studies may take a few weeks, while others—such as chronic toxicity tests—can run for several months. We provide realistic timelines and coordinate the process to keep things moving efficiently.

GLP studies can be a significant investment, but they are often mandatory for market access. We help you avoid unnecessary tests and design a cost-effective testing strategy that aligns with both your regulatory obligations and budget.