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.