All of our manufacturing and support operations are built on the framework of a comprehensive quality management system. Our quality management system is designed to ensure procedural and operational excellence across the organization.

The objectives of the Cytovance® Biologics' Quality Management System are:

  • To ensure compliance with relevant regulatory requirements (FDA, EMEA, ICH) throughout the product lifecycle

  • To ensure independent quality assurance oversight of all GMP activities

  • To provide phase specific quality control testing of product and material

  • To maximize customer satisfaction with all services provided support by providing compliant, complete, and timely records for GMP activities

  • To achieve and maintain a level of quality that enhances Cytovance® Biologics' reputation with current and future customers

Cytovance® Biologics recognizes its responsibility as a contract manufacturer to fully comply with all contractual and regulatory requirements. We are committed to customer satisfaction and continuous quality improvement.