The purpose of this document is to provide guidance for the use of Facility Identification Numbers found in a number of ISBT 128 data structures.

The purpose of this document is to provide guidance for implementation of the ISBT 128 Standard for blood transfusion in resource-limited countries. It is intended to provide options allowing facilities to promote safety, traceability, and efficiency without needing to implement all features of the ISBT 128 Standard.

The purpose of this document is to provide a mechanism to validate software reading bar-coded labels. Regulatory and compliance staff, as well as software developers, may find this guidance document helpful when developing certain validation test plans.

The purpose of this document is to provide guidance to help users implementing standardized labeling of collection products for further manufacture in compliance with the ISBT 128 Standard Labeling of Collection Products for Cellular Therapy Manufacturing (ST-018)

This document is intended to provide guidance to help users distribute ISBT 128 labeled products through a GS1 supply chain. It outlines how the ISBT 128 products can be packaged using a GS1 Serial Shipping Container Code (SSCC) and the associated ISBT 128 information can be incorporated into GS1 electronic dispatch information.

The purpose of this document is to provide a toolbox of commonly used items essential for implementing ISBT 128. It also provides guidance and recommended steps for consideration when planning out one’s ISBT 128 implementation.

The purpose of this document is to provide guidance on creating and using the MPHO Unique Identifier in compliance with the ISBT 128 Standard for the Medical Products of Human Origin (MPHO) Unique Identifier.