What is the CPC Biotech Validation Report?​

The CPC Biotech validation report provides the necessary information for your component review and approval process. CPC Biotech connectors are designed with ease-of-use and the operator in mind. This focus enables users to transfer fluids efficiently, reliably, and minimizing risk for operator error. Our robust designs provide reliable performance without the need for clamps, fixtures or tube welders. Biopharmaceutical manufacturers can make sterile connections with the quality and market availability they expect from the leader in single-use connection technology. A summary of the report can be found below:​

What is Included in the Validation Report?​

• Product Series Overview​
• Product Qualification Testing ​
• Microbial Ingress Testing (for sterile connect and disconnect technologies)​
• Material Biocompatibility Testing​

For information related to:​

• Regulations compliance, material content (e.g. animal content declarations), item surface areas, shelf life, and more please refer to the Supplier Qualification Guide. ​
• For an extractables study performed on CPC Biotech components used in bioprocessing applications, please reference the Extractables Report.​