Customizable, Reliable, Secure e-Delphyn® Cell Therapy Solution with integrated functionality to manage, control operations, increase productivity, and efficiency, handling donor recruitment to patient transfusion.
e-Delphyn Cell Therapy software supports the collection, processing, storage and distribution or administration of high-quality cellular therapy products. e-Delphyn Cellular Therapy is specifically developed for academic laboratories, cord blood banks and biotech companies who manufacture cell therapy, gene therapy, and immune therapy products. e-Delphyn Cellular Therapy is built to ensure quality and regulatory compliance.
Donor and Patient Safety
e-Delphyn offers an integrated suite of cell therapy solutions designed to track donor and patient records from point of registration to collections through manufacturing, storage, and final patient transfusion. Barcode and RFID technology is used extensively to identify Donor, Patients, and Products. Verification points in keys areas to ensure that the correct donor, product, and patient are delivered at all times.
Ease of Integration
Integration with other automated analyzers as well as Healthcare Information Systems is simple. e-Delphyn product suite is deployed with HL7, enabling easy integration with other systems such as HIS, LIS and other EMRs.
Our integrated suite is designed and updated to help to meet organizational stringent regulatory and accreditation requirements including AABB, FACT, ISBT 128 and more.
Managed Manufacturing Operations
e-Delphyn Cellular Therapy is designed to track inventoried item in the lab including all manufacturing consumables, equipments: lab instruments and freezers. Our software can link to organizational specific SOP’s to help ensure standardized processes and can be tailored to meet any given requirements.
Flexible and Secure Configuration
e-Delphyn Cell Therapy Solutions is designed to fit almost any operation structure. Security and access can be configured according to roles. Verification of various processes can be customized to suit a single level of approval or multiple levels of approvals. Every change in configuration is tracked and may be extracted for audit.