We design and conduct clinical trials for dietary supplements, cosmetics, and medical devices based on substances compliant with the European Regulation 2017/745 (MDR – Medical Device Regulation), and continuously collect market data to ensure the safety of our products.
We manage and conduct clinical studies on products, leveraging our extensive internal cross-disciplinary expertise. This enables us to collaborate effectively with various stakeholders: participants, ethics committees, competent authorities, scientific and academic societies. We constantly stay updated on increasingly stringent international regulations and guidelines to ensure the highest compliance and quality.
