Part D Administrative Contract Flowdowns

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Part D Administrative Contract Flowdowns By Kenneth M. Bruntel Crowell & Moring, LLP Presented to the American Health Lawyers Association Mid-Year Meeting Hollywood, FL May 2007

Threshold Question No. 1: What is a Flowdown? A statutory, regulatory, contractual, or other requirement imposed on Part D Plans that must or should also be imposed on certain PDP vendors Threshold Question No. 2: To Which Vendors Do Flowdowns Apply? No Part D guidance Draft Prescription Drug Benefit Manual Ch. 9 defined Subcontractor, but final Ch. 9 deleted definition and used downstream entity throughout 2

Who gets Part D Flowdowns? Every downstream entity? If not all, which ones? Managed Care Manual, Ch. 11, 100.5 (http://www.cms.hhs.gov/manuals/downloads/mc86c11. pdf ) core functions analysis: contract administration and management, marketing, utilization management, quality assurance, applications processing, enrollment and disenrollment functions, claims processing, adjudicating Medicare organization determinations, appeals and grievances, and credentialing Non-core functions, e.g., IT hardware and software, office, supplies, furniture, facilities, etc., excluded 3

Source of Flowdowns No one location Regulations Application Attestations Appendix V Certification Appendix VI Crosswalk Call Letter Contract 4

Regulatory Flowdowns 42 CFR 423.505(i) (2)(i) Audit rights (2)(ii) Document retention (3)(i) Enrollee protections (3)(ii) Accountability for delegations (3)(iii) Compliance with PDP contract requirements (4)(i) Written delegations and reporting (4)(ii) Remedies for unsatisfactory performance (4)(iii) Compliance with all applicable Federal laws, regulations and CMS instructions (5) PDP sponsor s right to approve, disapprove, or terminate delegated selection of providers 5

Regulatory Flowdowns - continued 42 CFR 423.505(j) Any other terms CMS finds necessary and appropriate 42 CFR 423.505(k) Certification of Claims Data if the claims data are generated by a subcontractor subcontractor must similarly certify (based on best knowledge, information and belief) the accuracy, completeness, and truthfulness of the data and acknowledge that the claims data will be used for the purpose of obtaining Federal reimbursement. 6

Part D Application (http://www.cms.hhs.gov/prescriptiondrugcovcontra/04 _RxContracting_ApplicationGuidance.asp#TopOfPage ) Attestations, e.g., 3.1.5. Business Integrity A.1. Applicant or subcontractors and subcontractor staff agree that they are bound by 46 CFR Part 76 and attest that they are not excluded. Appendix V Certification by Prescription Drug Plan Organization that Subcontracts Meet the Requirements of Section 3.1.2D and include: A.3 - Flowdown clauses from PDP contract A.8 - Compliance with Federal laws, etc. A.9 - Compliance with Federal and State privacy and security requirements A.10 - Contain all 42 CFR 423.505(i) requirements 7

Part D Application continued Appendix VI Crosswalk 8

Call Letter Flowdowns 2007 Part D call letter provides that contracts would require plan sponsors to submit financial and organizational conflicts of interest reports to CMS, pursuant to instructions to be issued by CMS. No such instructions forthcoming, except that Chapter 9 (Part D Program to Control Fraud Waste and Abuse), 50.2.1.2, p. 24 of the Prescription Drug Benefit Manual provides: the Sponsor should obtain certifications from first tier entities that these entities will require its managers, officers and directors responsible for the administration and delivery of Part D benefits to sign a conflict of interest statement, attestation, or certification at the time of hire and annually thereafter certifying that the manger, officer or director is free from any conflict of interest in administering or delivering Part D benefits. No such requirement in 2008 Combined Call Letter. 9

Additional Contract Flowdowns (MA-PD Contracts, H) Program Integrity The MA Organization agrees to provide notice based on best knowledge, information and belief to CMS of any integrity items related to payments from government entities, both federal and state, for healthcare or prescription drug services. These items include any investigations, legal actions or matters subject to arbitration brought involving the MA Organization (or MA Organization's firm if applicable) and its subcontractors (excluding contracted network providers), including any key management or executive staff, or any major shareholder (5% or more), by a government agency (state or federal) on matters relating to payments from government entities, both federal and state, for healthcare and/or prescription drug services. In providing the notice, the sponsor shall keep the government informed of when the integrity item is initiated and when it is closed. Notice should be provided of the details concerning any resolution and monetary payments as well as any settlement agreements or corporate integrity agreements. 10

Additional Contract Flowdowns (MA-PD Contracts, H) Program Integrity - continued The MA Organization agrees to provide notice based on best knowledge, information and belief to CMS in the event the MA Organization or any of its subcontractors is criminally convicted or has a civil judgment entered against it for fraudulent or is sanctioned under any Federal program involving the provision of health care or prescription drug services. 11