Legislation and standards of the pharmaceutical industry are designed to ensure that the final customer receives an effective, safe and high-quality medicinal products. Consequently, regardless of which stage of the medicinal product's lifecycle the company is involved, it must comply with regulatory requirements and comply with sectoral standards, whether it is pharmaceutical development, preclinical studies, clinical trials, manufacturing process, storage or distribution.
We understand the responsibility and the importance of adhering to high pharmaceutical standards to ensure the control of the supply chain, and thus to preserve the quality and integrity of products with marketing authorization or investigational medical products.
To this end, we have implemented a quality management system based on the international standard ISO 9001:2015, Good Distribution and Storage Practices,and Good Manufacturing Practice. Each stage in our activities is carried out under the supervision of experienced staff members of the Quality Assurance team. The effectiveness of the results of each process, from routine operations to strategic planning, is evaluated to improve the processes of the enterprise and services that fully meet the expectations of our customers.
Sergiy PomerantsevHead of Quality Control
