Sartorius Stedim Biotech has established multiple manufacturing sites with consistent industrial processes and state-of-the-art utilities. The expertise of designing single-use solutions based on collaborative supplier management and customer demand planning assures a flexible and robust supply chain that can cope with strong market growth.

Sartorius Stedim Biotech quality systems for single-use products follow applicable ISO and FDA regulations for medical devices. Design, manufacture and sterilization processes are conducted under conditions that mirror biopharmaceutical operations and meet cGMP requirements.