CPC engineers are constantly striving to find the right solution and they continue to raise the standards in sterile fluid handling. Getting validation right is extremely important in single-use manufacturing, given the highly regulated environment, the demand for lower drug costs and a multi-tiered supply chain. It takes collaboration and expertise along the supply chain to ensure the end product is validated.
Supply chains for single-use systems are presenting both manufacturers and end users with challenges. With increased regulatory scrutiny on supply chain security and risk mitigation strategies throughout the development and manufacture of therapeutic drug products, how can users ensure the expected level of compliance?