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Emdeon Recommends Secure Interim Solutions to Avert Delays in the Implementation of ePrescribing of Controlled Substances
Date:5/27/2010

jor barrier preventing certain physicians from ePrescribing as they will no longer have to maintain both paper and electronic workflows. Emdeon believes another benefit of ePrescribing of controlled substances to pharmacies, hospitals and practitioners will be the added level of security for controlled substance prescriptions that come with the new DEA regulations.

Emdeon's comments, which are both supportive and constructive, focus on the provisions that require a secure transmission of electronic prescriptions, including provisions relating to digital signature indicators and digital signatures; signing and transmitting prescriptions; content alteration and two-factor authentication. Emdeon's comments note that it believes the industry will take a significant amount of time to adopt and implement formal standards that address all parts of the Final Rule and suggests the DEA consider interim guidelines to support adoption variances. Emdeon believes such variances would permit quicker adoption while allowing the industry sufficient time to develop and implement long-term infrastructure to meet the minimum requirements of the Interim Final Rule.

"Security and data integrity are the most important factors driving the future success of ePrescribing of controlled substances," said Rick Sage, Emdeon's vice president of clinical services and the manager of Emdeon's participation in the MDPH research project. "Working in conjunction with our partners in the MDPH project, we successfully implemented a workable solution for electronic data transmission security. While the Interim Final Rule mandates some specific requirements that differ from the MDPH project, there are certainly enough similarities that will enable Emdeon to readily assist our partners in implementing and complying with the Final Rule."

Emdeon estimates only approximately 18% of al
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SOURCE Emdeon Inc.
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