Comprehensive Quality Assurance for Clinical Trials
Each study is conducted in accordance with the standards of Good Clinical Practice (GCP) and Good Laboratory Practice (GLP)
The Quality Assurance Unit (QAU) ensures adherence to internal regulations and monitors compliance throughout the clinical trial process. From the initial planning stages (study protocol) to study execution, documentation, and the compilation of the final report, every step is meticulously overseen to meet the highest standards.
Our commitment is to consistently meet and exceed customer and regulatory expectations. By adopting an ownership mindset, we carefully evaluate the impact of every decision, always prioritizing the integrity of the trial and the well-being of its participants.
Key highlights of our approach include:
- Strict adherence to ICH and GCP standards.
- Alignment with local and international regulatory requirements, leveraging regional expertise.
- A risk-based methodology to enhance compliance and efficiency.
By integrating industry best practices, we ensure that your clinical trial is conducted with precision, care, and a steadfast commitment to quality.