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42 U.S.C. § 1395w–115Subsidies for part D eligible individuals for qualified prescription drug coverage

submitted 91 years ago by Pub. L. 108-173 to r/title-42-THE-PUBLIC-HEALTH-AND-WELFARE · 3,796 words · no verdicts yet

in plain englishAI-generated · not legal advice

This section requires the Secretary to pay subsidies for qualifying prescription drug coverage for eligible individuals. It sets rules for direct subsidies, reinsurance, bid adjustments, payment methods, risk corridors, information use, fallback plans, and a temporary 2023 subsidy.

(a) Subsidy payment. To lower premiums for eligible individuals, limit adverse selection among prescription drug and MA–PD plans, and encourage sponsors and organizations to participate, the Secretary must pay the following subsidies to a PDP sponsor offering a prescription drug plan and to an MA organization offering an MA–PD plan. The overall subsidy for basic coverage is 74.5 percent, except that it is the percentage produced by section 1395w–113(a)(8) for 2024 through 2029 and, for 2030 and later, 100 percent minus the percentage specified in section 1395w–113(a)(9). (1) Direct subsidy. For each eligible individual enrolled in a prescription drug plan or MA–PD plan for a month, the Secretary must pay the plan’s standardized bid amount, adjusted under subsection (c)(1), minus the base beneficiary premium calculated under section 1395w–113(a)(2) or (8), as applicable, and adjusted under section 1395w–113(a)(1)(B). (2) Subsidy through reinsurance. The Secretary must also pay the reinsurance amount described in subsection (b). This section gives advance budget authority and obligates the Secretary to make these payments. (b) Reinsurance payment amount. (1) In general. For an eligible individual enrolled during a coverage year, the reinsurance payment is: (A) For a year before 2025, 80 percent of the allowable reinsurance costs described in paragraph (2) that are attributable to the portion of gross covered prescription drug costs described in paragraph (3) incurred after the individual’s costs exceed the annual out-of-pocket threshold in section 1395w–102(b)(4)(B). (B) For 2025 and later, the sum of— (i) for applicable drugs, 20 percent of the allowable reinsurance costs attributable to that portion of gross covered prescription drug costs incurred after the individual exceeds that annual threshold; and (ii) for covered part D drugs that are not applicable drugs, 40 percent of the allowable reinsurance costs attributable to that portion of gross covered prescription drug costs incurred after the individual exceeds that threshold. “Applicable drug” has the meaning given in section 1395w–114c(g)(2). This section does not define that term. (2) Allowable reinsurance costs. (A) Subject to subparagraph (B), “allowable reinsurance costs” means the part of gross covered prescription drug costs under a plan that the sponsor or organization, or the enrollee or someone acting for the enrollee, actually pays after discounts, chargebacks, and average percentage rebates. The amount may not exceed the part that would have been paid if the plan provided basic prescription drug coverage, or, for supplemental coverage, standard prescription drug coverage. This section does not define “discounts,” “chargebacks,” “average percentage rebates,” “basic prescription drug coverage,” or “standard prescription drug coverage.” (B) When applying subparagraph (A), allowable reinsurance costs include the part of an applicable drug’s negotiated price that a manufacturer paid under the manufacturer discount program in section 1395w–114c. “Negotiated price” is defined in section 1395w–114c(g)(6); this section does not define it. (3) Gross covered prescription drug costs. For an eligible individual enrolled during a coverage year, these are the costs incurred under the plan, excluding administrative costs but including costs directly related to dispensing covered part D drugs during the year and costs related to the deductible. Count the costs whether the individual or the plan pays them, and, for 2025 and later, whether a manufacturer pays them for an applicable drug. Count them whether or not the plan provides more than basic prescription drug coverage. (4) Coverage year defined. A coverage year is a calendar year in which covered part D drugs are dispensed, if the claim and payment for the claim are made within the period after the year ends that the Secretary specifies. (c) Adjustments relating to bids. (1) Health status risk adjustment. (A) Establishment of risk adjusters. The Secretary must establish a method to adjust the standardized bid amount under subsection (a)(1)(A) for differences in the costs of basic prescription drug coverage caused by differences in the actuarial risk of the enrollees served by different plans. The adjustment must not change the total amounts payable to the plans under subsection (a)(1), through the part of the monthly beneficiary premiums described in subsection (a)(1)(B), or through MA monthly prescription drug beneficiary premiums. (B) Considerations. In creating the method, the Secretary may consider similar methods used under section 1395w–23(a)(3) to adjust payments to MA organizations for original Medicare fee-for-service benefits. (C) Data collection. The Secretary must require (i) PDP sponsors to submit drug-claim data that can be linked for each person to part A and part B data, plus other information the Secretary finds necessary; and (ii) MA organizations offering MA–PD plans to submit drug-claim data that can be linked for each person to other data those organizations must submit to the Secretary, plus other information the Secretary finds necessary. (D) Publication. When the Secretary publishes risk-adjustment factors under section 1395w–23(b)(1)(B)(i)(II), the Secretary must publish the risk adjusters under this paragraph for the next year. (2) Geographic adjustment. (A) Subject to subparagraph (B), for section 1395w–113(a)(1)(B)(iii), the Secretary must establish a method to adjust the national average monthly bid amount calculated under section 1395w–113(a)(4) for price differences for covered part D drugs among PDP regions. (B) De minimis rule. If the Secretary decides those regional price differences are de minimis, the Secretary must not make an adjustment under this paragraph. “De minimis” is not defined in this section. (C) Budget neutral adjustment. The adjustment must not change the total payments under this part compared with the payments that would have been made without the adjustment. (d) Payment methods. (1) In general. Payments use a method the Secretary chooses. The Secretary may make interim payments during a year based on the best estimate of what will be payable after all information is obtained. (2) Requirement for provision of information. (A) Requirement. Payment to a PDP sponsor or MA organization depends on furnishing the Secretary, in the form and manner the Secretary specifies, the information needed to carry out this section. (B) Restriction on use. Officers, employees, and contractors of the Department of Health and Human Services may use information provided or obtained under subparagraph (A) only to carry out this section and only as necessary for that purpose. (3) Source of payments. Payments come from the Medicare Prescription Drug Account. (4) Application of enrollee adjustment. Section 1395w–23(a)(2) applies to payments to PDP sponsors under this section in the same way it applies to payments to MA organizations under section 1395w–23(a). (e) Portion of total payments subject to risk (risk corridors). (1) Computation of adjusted allowable risk-corridor costs. (A) “Adjusted allowable risk-corridor costs” for a plan and coverage year means the plan’s allowable risk-corridor costs under subparagraph (B), minus (I) all reinsurance payments under subsection (b) to the plan’s sponsor for the year and (II) all subsidy payments under section 1395w–114 to that sponsor for the year. (B) “Allowable risk-corridor costs” means the plan costs, excluding administrative costs but including costs directly related to dispensing covered part D drugs, that the sponsor or organization actually pays after discounts, chargebacks, and average percentage rebates. The costs may not exceed what would have been paid if the coverage were basic coverage or, for supplemental coverage, basic coverage with the adjustment under section 1395w–111(c)(2). The Secretary must calculate these costs using the maximum copayments allowed under section 1395w–114(a)(1)(D) and (2)(E). (2) Adjustment of payment. (A) No adjustment inside corridor. If adjusted allowable risk-corridor costs are at least the first lower threshold and no more than the first upper threshold established in paragraph (3), the Secretary makes no payment adjustment. (B) Increase above upper limit. (i) Between the first and second upper thresholds. If costs are above the first upper threshold but no more than the second, the Secretary increases the plan’s total payments by 50 percent of the difference between the costs and the first upper threshold. For 2006 and 2007, the percentage is 75 percent or 90 percent if clause (iii)’s conditions are met. (ii) Above the second upper threshold. If costs exceed the second upper threshold, the increase is the sum of 50 percent of the difference between the second and first upper thresholds, plus 80 percent of the difference between the costs and the second upper threshold. For 2006 and 2007, the first percentage is 75 percent or 90 percent if clause (iii)’s conditions are met. (iii) Conditions for the higher 2006 and 2007 percentage. The conditions are met if the Secretary determines that, in that year, at least 60 percent of the covered prescription drug and MA–PD plans have costs above their first upper threshold and those plans include at least 60 percent of eligible individuals enrolled in any such plan. (C) Reduction below lower limit. (i) Between the first and second lower thresholds. If costs are below the first lower threshold but at least the second lower threshold, the Secretary reduces payments, or otherwise recovers money, by 50 percent of the difference between the first lower threshold and the costs. For 2006 and 2007, the percentage is 75 percent. (ii) Below the second lower threshold. If costs are below the second lower threshold, the reduction or recovery is the sum of 50 percent of the difference between the first and second lower thresholds, plus 80 percent of the difference between the second upper threshold and the costs. For 2006 and 2007, the first percentage is 75 percent. (3) Establishment of risk corridors. (A) In general. For each plan year, the Secretary must establish a corridor for each prescription drug plan and MA–PD plan. (i) First lower threshold: the target amount in subparagraph (B) minus the first threshold risk percentage under subparagraph (C)(i) multiplied by that target amount. (ii) Second lower threshold: the target amount minus the second threshold risk percentage under subparagraph (C)(ii) multiplied by that target amount. (iii) First upper threshold: the target amount plus the amount subtracted in clause (i)(II). (iv) Second upper threshold: the target amount plus the amount subtracted in clause (ii)(II). (B) Target amount. The target amount is the total payments for the plan for the year to its PDP sponsor or MA organization, including amounts paid by the Secretary and enrollees, based on the risk-adjusted standardized bid amount. It is reduced by the administrative expenses for the year assumed in that bid. (C) First and second threshold risk percentages. (i) The first percentage is 2.5 percent for 2006 and 2007, 5 percent for 2008 through 2011, and a percentage set by the Secretary for 2012 and later, never below 5 percent. (ii) The second percentage is 5 percent for 2006 and 2007, 10 percent for 2008 through 2011, and a percentage set by the Secretary for 2012 and later that is greater than the first percentage for that year and never below 10 percent. (iii) To help ensure two plans in an area, a PDP sponsor may, under section 1395w–111(b)(2)(E)(ii), submit a bid asking to lower the applicable first or second percentage or raise the percentages used in paragraph (2). (4) Plans at risk for all supplemental coverage. A PDP sponsor and MA organization offering supplemental prescription drug benefits bears all financial risk for providing those supplemental benefits. (5) No effect on monthly premium. A payment adjustment under this subsection does not change the monthly beneficiary premium or the MA monthly prescription drug beneficiary premium. (f) Disclosure of information. (1) In general. Every contract under this part or part C must require that (A) the PDP sponsor or MA organization provide the Secretary with information the Secretary finds necessary to carry out this section; and (B) the Secretary may inspect and audit the sponsor’s or organization’s books and records concerning the cost information, under section 1395w–27(d)(2)(B) as applied by section 1395w–112(b)(3)(C). (2) Restriction on use. Information disclosed or obtained under this section may be used by HHS officers, employees, and contractors only as needed to carry out this section or part E of subchapter XI and to oversee, evaluate, and enforce this subchapter; by the Attorney General and Comptroller General only as needed for health oversight; by the executive directors of MedPAC and MACPAC for the monitoring, recommendations, and analysis described in the statute; and by the Congressional Budget Office Director for analysis of programs authorized under this chapter and performance of duties under the Congressional Budget and Impoundment Control Act of 1974. (3) Additional disclosure restrictions. (A) The executive directors just described may not disclose, for a prescription drug or MA–PD plan: (i) the specific amounts or sources of rebates, discounts, price concessions, or other direct or indirect remuneration; (ii) information submitted with the sponsor’s section 1395w–111(b) bid or organization’s section 1395w–24(a) bid; or (iii) prescription drug event-record information in a form that CMS could not release under 42 C.F.R. § 423.505(m) or a successor rule. (B) The same restrictions apply to disclosures to individual commissioners of MedPAC or MACPAC. (g) Payment for fallback prescription drug plans. Instead of the amounts otherwise payable under this section to a sponsor offering a fallback plan, the amount payable is the amount determined under the plan’s contract under sections 1395w–111(g)(4) and (5). (h) Temporary retrospective subsidy for reduced cost-sharing and deductibles for certain adult vaccines and insulin during 2023. (1) In addition to other payments for plan year 2023, the Secretary must pay a PDP sponsor or MA organization a subsidy equal to the total reduction in cost-sharing and deductibles for individuals under the plan caused by section 1395w–102(b)(8) or (9). (2) Timing. The Secretary must provide the subsidy, as applicable, no later than 18 months after the applicable plan year ends.
the actual law source: uscode.house.gov ↗public domain
(a) Subsidy payment

In order to reduce premium levels applicable to qualified prescription drug coverage for part D eligible individuals consistent with an overall subsidy level of 74.5 percent (or, for each of 2024 through 2029, the percent applicable as a result of the application of section 1395w–113(a)(8) of this title, or, for 2030 and each subsequent year, 100 percent minus the percent specified under section 1395w–113(a)(9) of this title) for basic prescription drug coverage, to reduce adverse selection among prescription drug plans and MA–PD plans, and to promote the participation of PDP sponsors under this part and MA organizations under part C, the Secretary shall provide for payment to a PDP sponsor that offers a prescription drug plan and an MA organization that offers an MA–PD plan of the following subsidies in accordance with this section:

(1) Direct subsidy

A direct subsidy for each part D eligible individual enrolled in a prescription drug plan or MA–PD plan for a month equal to—

(A)

the amount of the plan’s standardized bid amount (as defined in section 1395w–113(a)(5) of this title), adjusted under subsection (c)(1), reduced by

(B)

the base beneficiary premium (as computed under paragraph (2) or (8) of section 1395w–113(a) of this title (as applicable) and as adjusted under paragraph (1)(B) of such section).

(2) Subsidy through reinsurance

The reinsurance payment amount (as defined in subsection (b)).

This section constitutes budget authority in advance of appropriations Acts and represents the obligation of the Secretary to provide for the payment of amounts provided under this section.

(b) Reinsurance payment amount
(1) In general

The reinsurance payment amount under this subsection for a part D eligible individual enrolled in a prescription drug plan or MA–PD plan for a coverage year is an amount equal to—

(A)

for a year preceding 2025, 80 percent of the allowable reinsurance costs (as specified in paragraph (2)) attributable to that portion of gross covered prescription drug costs as specified in paragraph (3) incurred in the coverage year after such individual has incurred costs that exceed the annual out-of-pocket threshold specified in section 1395w–102(b)(4)(B) of this title; and

(B)

for 2025 and each subsequent year, the sum of—

(i)

with respect to applicable drugs (as defined in section 1395w–114c(g)(2) of this title), an amount equal to 20 percent of such allowable reinsurance costs attributable to that portion of gross covered prescription drug costs as specified in paragraph (3) incurred in the coverage year after such individual has incurred costs that exceed the annual out-of-pocket threshold specified in section 1395w–102(b)(4)(B) of this title; and

(ii)

with respect to covered part D drugs that are not applicable drugs (as so defined), an amount equal to 40 percent of such allowable reinsurance costs attributable to that portion of gross covered prescription drug costs as specified in paragraph (3) incurred in the coverage year after such individual has incurred costs that exceed the annual out-of-pocket threshold specified in section 1395w–102(b)(4)(B) of this title.

(2) Allowable reinsurance costs
(A) In general

Subject to subparagraph (B), for purposes of this section, the term “allowable reinsurance costs” means, with respect to gross covered prescription drug costs under a prescription drug plan offered by a PDP sponsor or an MA–PD plan offered by an MA organization, the part of such costs that are actually paid (net of discounts, chargebacks, and average percentage rebates) by the sponsor or organization or by (or on behalf of) an enrollee under the plan, but in no case more than the part of such costs that would have been paid under the plan if the prescription drug coverage under the plan were basic prescription drug coverage, or, in the case of a plan providing supplemental prescription drug coverage, if such coverage were standard prescription drug coverage.

(B) Inclusion of manufacturer discounts on applicable drugs

For purposes of applying subparagraph (A), the term “allowable reinsurance costs” shall include the portion of the negotiated price (as defined in section 1395w–114c(g)(6) of this title) of an applicable drug (as defined in section 1395w–114c(g)(2) of this title) that was paid by a manufacturer under the manufacturer discount program under section 1395w–114c of this title.

(3) Gross covered prescription drug costs

Subject to paragraph (2)(B), for purposes of this section, the term “gross covered prescription drug costs” means, with respect to a part D eligible individual enrolled in a prescription drug plan or MA–PD plan during a coverage year, the costs incurred under the plan, not including administrative costs, but including costs directly related to the dispensing of covered part D drugs during the year and costs relating to the deductible. Such costs shall be determined whether they are paid by the individual or under the plan (or, with respect to 2025 and subsequent years, in the case of an applicable drug, as defined in section 1395w–114c(g)(2) of this title, by a manufacturer), regardless of whether the coverage under the plan exceeds basic prescription drug coverage.

(4) Coverage year defined

For purposes of this section, the term “coverage year” means a calendar year in which covered part D drugs are dispensed if the claim for such drugs (and payment on such claim) is made not later than such period after the end of such year as the Secretary specifies.

(c) Adjustments relating to bids
(1) Health status risk adjustment
(A) Establishment of risk adjustors

The Secretary shall establish an appropriate methodology for adjusting the standardized bid amount under subsection (a)(1)(A) to take into account variation in costs for basic prescription drug coverage among prescription drug plans and MA–PD plans based on the differences in actuarial risk of different enrollees being served. Any such risk adjustment shall be designed in a manner so as not to result in a change in the aggregate amounts payable to such plans under subsection (a)(1) and through that portion of the monthly beneficiary prescription drug premiums described in subsection (a)(1)(B) and MA monthly prescription drug beneficiary premiums.

(B) Considerations

In establishing the methodology under subparagraph (A), the Secretary may take into account the similar methodologies used under section 1395w–23(a)(3) of this title to adjust payments to MA organizations for benefits under the original medicare fee-for-service program option.

(C) Data collection

In order to carry out this paragraph, the Secretary shall require—

(i)

PDP sponsors to submit data regarding drug claims that can be linked at the individual level to part A and part B data and such other information as the Secretary determines necessary; and

(ii)

MA organizations that offer MA–PD plans to submit data regarding drug claims that can be linked at the individual level to other data that such organizations are required to submit to the Secretary and such other information as the Secretary determines necessary.

(D) Publication

At the time of publication of risk adjustment factors under section 1395w–23(b)(1)(B)(i)(II) of this title, the Secretary shall publish the risk adjusters established under this paragraph for the succeeding year.

(2) Geographic adjustment
(A) In general

Subject to subparagraph (B), for purposes of section 1395w–113(a)(1)(B)(iii) of this title, the Secretary shall establish an appropriate methodology for adjusting the national average monthly bid amount (computed under section 1395w–113(a)(4) of this title) to take into account differences in prices for covered part D drugs among PDP regions.

(B) De minimis rule

If the Secretary determines that the price variations described in subparagraph (A) among PDP regions are de minimis, the Secretary shall not provide for adjustment under this paragraph.

(C) Budget neutral adjustment

Any adjustment under this paragraph shall be applied in a manner so as to not result in a change in the aggregate payments made under this part that would have been made if the Secretary had not applied such adjustment.

(d) Payment methods
(1) In general

Payments under this section shall be based on such a method as the Secretary determines. The Secretary may establish a payment method by which interim payments of amounts under this section are made during a year based on the Secretary’s best estimate of amounts that will be payable after obtaining all of the information.

(2) Requirement for provision of information
(A) Requirement

Payments under this section to a PDP sponsor or MA organization are conditioned upon the furnishing to the Secretary, in a form and manner specified by the Secretary, of such information as may be required to carry out this section.

(B) Restriction on use of information

Information disclosed or obtained pursuant to subparagraph (A) may be used by officers, employees, and contractors of the Department of Health and Human Services only for the purposes of, and to the extent necessary in, carrying out this section.

(3) Source of payments

Payments under this section shall be made from the Medicare Prescription Drug Account.

(4) Application of enrollee adjustment

The provisions of section 1395w–23(a)(2) of this title shall apply to payments to PDP sponsors under this section in the same manner as they apply to payments to MA organizations under section 1395w–23(a) of this title.

(e) Portion of total payments to a sponsor or organization subject to risk (application of risk corridors)
(1) Computation of adjusted allowable risk corridor costs
(A) In general

For purposes of this subsection, the term “adjusted allowable risk corridor costs” means, for a plan for a coverage year (as defined in subsection (b)(4))—

(i)

the allowable risk corridor costs (as defined in subparagraph (B)) for the plan for the year, reduced by

(ii)

the sum of (I) the total reinsurance payments made under subsection (b) to the sponsor of the plan for the year, and (II) the total subsidy payments made under section 1395w–114 of this title to the sponsor of the plan for the year.

(B) Allowable risk corridor costs

For purposes of this subsection, the term “allowable risk corridor costs” means, with respect to a prescription drug plan offered by a PDP sponsor or an MA–PD plan offered by an MA organization, the part of costs (not including administrative costs, but including costs directly related to the dispensing of covered part D drugs during the year) incurred by the sponsor or organization under the plan that are actually paid (net of discounts, chargebacks, and average percentage rebates) by the sponsor or organization under the plan, but in no case more than the part of such costs that would have been paid under the plan if the prescription drug coverage under the plan were basic prescription drug coverage, or, in the case of a plan providing supplemental prescription drug coverage, if such coverage were basic prescription drug coverage taking into account the adjustment under section 1395w–111(c)(2) of this title. In computing allowable costs under this paragraph, the Secretary shall compute such costs based upon imposition under paragraphs (1)(D) and (2)(E) of section 1395w–114(a) of this title of the maximum amount of copayments permitted under such paragraphs.

(2) Adjustment of payment
(A) No adjustment if adjusted allowable risk corridor costs within risk corridor

If the adjusted allowable risk corridor costs (as defined in paragraph (1)) for the plan for the year are at least equal to the first threshold lower limit of the risk corridor (specified in paragraph (3)(A)(i)), but not greater than the first threshold upper limit of the risk corridor (specified in paragraph (3)(A)(iii)) for the plan for the year, then no payment adjustment shall be made under this subsection.

(B) Increase in payment if adjusted allowable risk corridor costs above upper limit of risk corridor
(i) Costs between first and second threshold upper limits

If the adjusted allowable risk corridor costs for the plan for the year are greater than the first threshold upper limit, but not greater than the second threshold upper limit, of the risk corridor for the plan for the year, the Secretary shall increase the total of the payments made to the sponsor or organization offering the plan for the year under this section by an amount equal to 50 percent (or, for 2006 and 2007, 75 percent or 90 percent if the conditions described in clause (iii) are met for the year) of the difference between such adjusted allowable risk corridor costs and the first threshold upper limit of the risk corridor.

(ii) Costs above second threshold upper limits

If the adjusted allowable risk corridor costs for the plan for the year are greater than the second threshold upper limit of the risk corridor for the plan for the year, the Secretary shall increase the total of the payments made to the sponsor or organization offering the plan for the year under this section by an amount equal to the sum of—

(I)

50 percent (or, for 2006 and 2007, 75 percent or 90 percent if the conditions described in clause (iii) are met for the year) of the difference between the second threshold upper limit and the first threshold upper limit; and

(II)

80 percent of the difference between such adjusted allowable risk corridor costs and the second threshold upper limit of the risk corridor.

(iii) Conditions for application of higher percentage for 2006 and 2007

The conditions described in this clause are met for 2006 or 2007 if the Secretary determines with respect to such year that—

(I)

at least 60 percent of prescription drug plans and MA–PD plans to which this subsection applies have adjusted allowable risk corridor costs for the plan for the year that are more than the first threshold upper limit of the risk corridor for the plan for the year; and

(II)

such plans represent at least 60 percent of part D eligible individuals enrolled in any prescription drug plan or MA–PD plan.

(C) Reduction in payment if adjusted allowable risk corridor costs below lower limit of risk corridor
(i) Costs between first and second threshold lower limits

If the adjusted allowable risk corridor costs for the plan for the year are less than the first threshold lower limit, but not less than the second threshold lower limit, of the risk corridor for the plan for the year, the Secretary shall reduce the total of the payments made to the sponsor or organization offering the plan for the year under this section by an amount (or otherwise recover from the sponsor or organization an amount) equal to 50 percent (or, for 2006 and 2007, 75 percent) of the difference between the first threshold lower limit of the risk corridor and such adjusted allowable risk corridor costs.

(ii) Costs below second threshold lower limit

If the adjusted allowable risk corridor costs for the plan for the year are less the second threshold lower limit of the risk corridor for the plan for the year, the Secretary shall reduce the total of the payments made to the sponsor or organization offering the plan for the year under this section by an amount (or otherwise recover from the sponsor or organization an amount) equal to the sum of—

(I)

50 percent (or, for 2006 and 2007, 75 percent) of the difference between the first threshold lower limit and the second threshold lower limit; and

(II)

80 percent of the difference between the second threshold upper limit of the risk corridor and such adjusted allowable risk corridor costs.

(3) Establishment of risk corridors
(A) In general

For each plan year the Secretary shall establish a risk corridor for each prescription drug plan and each MA–PD plan. The risk corridor for a plan for a year shall be equal to a range as follows:

(i) First threshold lower limit

The first threshold lower limit of such corridor shall be equal to—

(I)

the target amount described in subparagraph (B) for the plan; minus

(II)

an amount equal to the first threshold risk percentage for the plan (as determined under subparagraph (C)(i)) of such target amount.

(ii) Second threshold lower limit

The second threshold lower limit of such corridor shall be equal to—

(I)

the target amount described in subparagraph (B) for the plan; minus

(II)

an amount equal to the second threshold risk percentage for the plan (as determined under subparagraph (C)(ii)) of such target amount.

(iii) First threshold upper limit

The first threshold upper limit of such corridor shall be equal to the sum of—

(I)

such target amount; and

(II)

the amount described in clause (i)(II).

(iv) Second threshold upper limit

The second threshold upper limit of such corridor shall be equal to the sum of—

(I)

such target amount; and

(II)

the amount described in clause (ii)(II).

(B) Target amount described

The target amount described in this paragraph is, with respect to a prescription drug plan or an MA–PD plan in a year, the total amount of payments paid to the PDP sponsor or MA–PD organization for the plan for the year, taking into account amounts paid by the Secretary and enrollees, based upon the standardized bid amount (as defined in section 1395w–113(a)(5) of this title and as risk adjusted under subsection (c)(1)), reduced by the total amount of administrative expenses for the year assumed in such standardized bid.

(C) First and second threshold risk percentage defined
(i) First threshold risk percentage

Subject to clause (iii), for purposes of this section, the first threshold risk percentage is—

(I)

for 2006 and 2007, and 1 2.5 percent;

(II)

for 2008 through 2011, 5 percent; and

(III)

for 2012 and subsequent years, a percentage established by the Secretary, but in no case less than 5 percent.

(ii) Second threshold risk percentage

Subject to clause (iii), for purposes of this section, the second threshold risk percentage is—

(I)

for 2006 and 2007, 5 percent;

(II)

for 2008 through 2011, 10 percent; and

(III)

for 2012 and subsequent years, a percentage established by the Secretary that is greater than the percent established for the year under clause (i)(III), but in no case less than 10 percent.

(iii) Reduction of risk percentage to ensure 2 plans in an area

Pursuant to section 1395w–111(b)(2)(E)(ii) of this title, a PDP sponsor may submit a bid that requests a decrease in the applicable first or second threshold risk percentages or an increase in the percents applied under paragraph (2).

(4) Plans at risk for entire amount of supplemental prescription drug coverage

A PDP sponsor and MA organization that offers a plan that provides supplemental prescription drug benefits shall be at full financial risk for the provision of such supplemental benefits.

(5) No effect on monthly premium

No adjustment in payments made by reason of this subsection shall affect the monthly beneficiary premium or the MA monthly prescription drug beneficiary premium.

(f) Disclosure of information
(1) In general

Each contract under this part and under part C shall provide that—

(A)

the PDP sponsor offering a prescription drug plan or an MA organization offering an MA–PD plan shall provide the Secretary with such information as the Secretary determines is necessary to carry out this section; and

(B)

the Secretary shall have the right in accordance with section 1395w–27(d)(2)(B) of this title (as applied under section 1395w–112(b)(3)(C) of this title) to inspect and audit any books and records of a PDP sponsor or MA organization that pertain to the information regarding costs provided to the Secretary under subparagraph (A).

(2) Restriction on use of information

Information disclosed or obtained pursuant to the provisions of this section may be used—

(A)

by officers, employees, and contractors of the Department of Health and Human Services for the purposes of, and to the extent necessary in—

(i)

carrying out this section or part E of subchapter XI; and

(ii)

conducting oversight, evaluation, and enforcement under this subchapter;

(B)

by the Attorney General and the Comptroller General of the United States for the purposes of, and to the extent necessary in, carrying out health oversight activities;

(C)

by the Executive Director of the Medicare Payment Advisory Commission for purposes of monitoring, making recommendations for, and analysis of the program under this subchapter and by the Executive Director of the Medicaid and CHIP Payment and Access Commission for purposes of monitoring, making recommendations for, and analysis of the Medicaid program established under subchapter XIX and the Children’s Health Insurance Program under subchapter XXI; and

(D)

by the Director of the Congressional Budget Office for the purposes of analysis of programs authorized under this chapter, as applicable, and the fulfilment of such Director’s duties under the Congressional Budget and Impoundment Control Act of 1974.

(3) Additional restrictions on disclosure of information
(A) In general

The Executive Directors described in paragraph (2)(C) shall not disclose any of the following information disclosed to such Executive Directors or obtained by such Executive Directors pursuant to such paragraph, with respect to a prescription drug plan offered by a PDP sponsor or an MA–PD plan offered by an MA organization:

(i)

The specific amounts or the identity of the source of any rebates, discounts, price concessions, or other forms of direct or indirect remuneration under such prescription drug plan or such MA–PD plan.

(ii)

Information submitted with the bid submitted under section 1395w–111(b) of this title by such PDP sponsor or under section 1395w–24(a) of this title by such MA organization.

(iii)

In the case of such information from prescription drug event records, information in a form that would not be permitted under section 423.505(m) of title 42, Code of Federal Regulations, or any successor regulation, if released by the Centers for Medicare & Medicaid Services.

(B) Clarification

The restrictions on disclosures described in subparagraph (A) shall also apply to disclosures to individual Commissioners of the Medicare Payment Advisory Commission or of the Medicaid and CHIP Payment and Access Commission.

(g) Payment for fallback prescription drug plans

In lieu of the amounts otherwise payable under this section to a PDP sponsor offering a fallback prescription drug plan (as defined in section 1395w–111(g)(4) of this title2), the amount payable shall be the amounts determined under the contract for such plan pursuant to section 1395w–111(g)(5) of this title.

(h) Temporary retrospective subsidy for reduction in cost-sharing and deductible for adult vaccines recommended by the Advisory Committee on Immunization Practices and Insulin During 2023
(1) In general

In addition to amounts otherwise payable under this section to a PDP sponsor of a prescription drug plan or an MA organization offering an MA–PD plan, for plan year 2023, the Secretary shall provide the PDP sponsor or MA organization offering the plan subsidies in an amount equal to the aggregate reduction in cost-sharing and deductible by reason of the application of paragraph (8) or (9) of section 1395w–102(b) of this title for individuals under the plan during the year.

(2) Timing

The Secretary shall provide a subsidy under paragraph (1), as applicable, not later than 18 months following the end of the applicable plan year.

Source credit: (Aug. 14, 1935, ch. 531, title XVIII, § 1860D–15, as added Pub. L. 108–173, title I, § 101(a)(2), Dec. 8, 2003, 117 Stat. 2113; amended Pub. L. 111–148, title VI, § 6402(b)(1), Mar. 23, 2010, 124 Stat. 756; Pub. L. 116–260, div. CC, title I, § 112(a), Dec. 27, 2020, 134 Stat. 2946; Pub. L. 117–169, title I, §§ 11001(b)(1)(H)(ii), 11201(b), (d)(3)(D), 11401(c)(1), 11406(c), Aug. 16, 2022, 136 Stat. 1853, 1879, 1891, 1897, 1904; Pub. L. 117–328, div. FF, title IV, § 4132, Dec. 29, 2022, 136 Stat. 5918.)

history & why it existsrecord from the source credit
  • 1935Enacted · Pub. L. 108-173 · 117 Stat. 2113
  • 2010Amended · Pub. L. 111-148 · 124 Stat. 756
  • 2020Amended · Pub. L. 116-260 · 134 Stat. 2946
  • 2022Amended · Pub. L. 117-169 · 136 Stat. 1853, 1879, 1891, 1897, 1904
  • 2022Amended · Pub. L. 117-328 · 136 Stat. 5918

A history note hasn’t been published yet. The record shows enactment by Pub. L. 108-173 on 1935-08-14.

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