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ISBT 128 Clinical Trials Product Description Codes were specifically developed for the identification and labeling of clinical trials products. These Clinical Trials PDCs are standardized global identifiers allocated by ICCBBA, which may be used by organizations licensed with ICCBBA, including clinical trials facilities, clinical trial sponsors, and cell and gene therapy manufacturers.

The purpose of this video is to explain the difference between ISBT 128 product information that is encoded versus the text printed on the label.

Presentation Outline:

• An overview of the structure of the ISBT 128 Delivery Mechanisms e.g., Code 128 Barcode and 2D Data Matrix
• Label examples that demonstrate the distinction between barcoded information and printed text

The purpose of this video is to show how the ISBT 128 Donation Identification Numbers (DIN) and Product Codes support traceability, as well as how the Facility Identification Number (FIN) is used within the DIN.

Presentation Outline:

• Overview of ISBT 128 Donation Identification Number (DIN) and Product Code
• How the Facility Identification Number (FIN) is used within the (DIN)
• How the (DIN) and Product support traceability for ISBT 128

The purpose of this video is to provide information to European Tissue Establishments that are working towards implementation of the SEC for tissues and cells. It assumes that the audience is already familiar with the European Directive on tissues and cells, including Commission Directive 2015/565 of April 2015.

Presentation Outline:

• Background to the ISBT 128 Standard
• Current global status of the use of ISBT 128
• Information on ICCBBA (An NGO in official relations with WHO)
• Implementation steps required for SEC
• The benefits of introducing ISBT 128 alongside the SEC

The purpose of this video is to provide a brief overview of the ISBT 128 Standard.​

Presentation Outline:

• Background to the ISBT 128 Standard
• What is ISBT 128
• The Information Environment
• The Role of ICCBBA