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GLP Services

Good Laboratory Practice (GLP) defines a rigorous quality system that governs the planning, execution, monitoring, documentation, reporting, and archiving of non-clinical health and environmental safety studies. It ensures that studies are conducted with uniformity, consistency, reliability, reproducibility, quality, and integrity.

Academic research groups that want to advance the development of innovative products and medical devices must be able to navigate the complex regulatory approval process to prepare the products for market readiness. Advancing the development of these inventions beyond the research stage will lead to higher success rates in commercialization (e.g., spin-offs, licensing) and thus to greater opportunities for clinical application.

A GLP-compliant quality management system helps bridge this critical gap, supporting the regulatory readiness of academic innovations and facilitating their clinical translation and commercial viability.

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