Quality Assurance
Each study is conducted in accordance with the standards of Good Clinical Practice (GCP) and Good Laboratory Practice (GLP).
The Quality Assurance Unit (QAU) proceeds according to internal regulations and monitors compliance at every step, from planning (study protocol) and conducting the study to documentation and compilation of the final report.
Our approach is centered on consistently meeting and surpassing both customer and regulatory expectations. We adopt an ownership mentality, carefully evaluating the impact of every decision and prioritizing the best interests of the trial and its participants, while ensuring strict adherence to applicable standards and regulations.
Embedded in our operations is the agility and technological capability to meet regulatory standards and adapt to the evolving demands of studies. We prioritize compliance, data integrity, and the safety of your trial. Our practices are always aligned with ICH and GCP standards, as well as relevant regulatory requirements and guidelines in the regions where we operate, ensuring compliance with local regulations by leveraging local expertise and employing a risk-based approach.