Texas Instruments and VeriSign Joint RFID Model

TI and Verisign released a white paper in June 2005 that provided a trusted RFID model for the pharmaceutical industry . The combination of R FID and PKI technology has added a new layer of security and effectively counterfeited counterfeit drugs.

In order to combat counterfeit drugs in the pharmaceutical circulation field, TI and Verisign released a white paper in June 2005 to provide the pharmaceutical industry with an identifiable RFID model. The model proposes an improvement on the real-time safety of item-level products: by creating a higher level of authentication between the tag and any identifiable RFID reader (placed from the manufacturing site to the point of sale).

This model uses ISO/IEC standard 13.56 MHz RFID and PKI public key technologies and plans to complete the fight against counterfeit drugs in two phases. TI's and VeriSign 's identifiable RFID models can identify individual drugs, as well as confirm all drug transactions within the surveillance system beyond the working hours of the circulation infrastructure.

The characteristic of this model is that from the production of medicines to the sale of medicines, there are identifiable RFID readers and labels to identify the finished medicines, thereby strengthening the real-time identification level and enhancing the safety of the medicines. 3M , a leading provider of security solutions including RFID tracking and authentication systems, will provide credited RFID readers to support this new model. The purpose of the development of this technology is to prevent the circulation of counterfeit and inferior drugs on the market through stricter monitoring of drug production and distribution systems.

This RFID model uses real-time, off-grid authentication technology to monitor the drug distribution department. This monitoring can be quickly implemented using the existing infrastructure with minimal investment. By RFID  


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