Serocon Ar-Ge Biyoteknoloji Sağlık Kimya Ticaret Anonim Şirketi

As a manufacturer of quality control materials for clinical laboratories, Serocon provides solutions supporting both internal quality control and external quality assessment processes.

Our portfolio includes a broad range of human-derived control materials developed to support consistent and reliable laboratory performance across different areas of clinical diagnostics. With a focus on stability, usability and laboratory needs, Serocon offers quality control solutions designed for long-term performance monitoring.

In addition to its standard portfolio, Serocon provides flexible manufacturing capabilities for specific parameters and program requirements, particularly within external quality assessment applications.

In line with the evolving requirements of the European In Vitro Diagnostic Medical Devices Regulation (IVDR – Regulation (EU) 2017/746), Serocon continues to strengthen its quality, documentation and regulatory processes to support the expectations of modern diagnostic laboratories and international markets.

Serocon Portal complements these solutions by enabling laboratories to monitor results, evaluate performance trends and compare their data within broader participant groups through a centralized digital platform.

By combining laboratory-focused manufacturing expertise, regulatory awareness and digital quality assessment tools, Serocon delivers reliable, adaptable and internationally oriented quality control solutions for laboratories worldwide.