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<strong>CMS</strong>-1403-FC<br />

ability of an electronic prescribing system to receive<br />

tiered formulary information, if available, would suffice<br />

for this requirement for 2009 and until this function is<br />

more widely available in the marketplace.<br />

(d) Provide information on formulary or tiered<br />

formulary medications, patient eligibility, and<br />

authorization requirements received electronically from the<br />

patient’s drug plan (if available).<br />

Part D E-Prescribing Standards. Section<br />

1848(m)(3)(B)(v) of the Act, as redesignated and added by<br />

the MIPPA, requires that, to the extent practicable, “the<br />

Secretary shall ensure that eligible professionals utilize<br />

electronic prescribing systems in compliance with standards<br />

established for such systems pursuant to the Part D<br />

Electronic Prescribing Program under section 1860D-4(e) of<br />

the Act.” Part D sponsors must use when they transmit<br />

prescriptions and certain prescription related information<br />

for Part D covered drugs that are prescribed for Part D<br />

eligible individuals. In the qualified electronic<br />

prescribing system context of this rule, electronic systems<br />

must convey the information listed above under (a) through<br />

(d) using the standards currently in effect for the Part D<br />

e-prescribing program. New Part D e-prescribing standards<br />

will be effective April 1, 2009. These new Part D e-<br />

689

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