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HHSCMS
  • ByLearn Laws®
  • Published09/02/2026
  • Updated09/02/2026

CMS Seeks Public Comment on Critical Information Collections for Medicaid Managed Care and Money Follows the Person Programs


The Centers for Medicare & Medicaid Services, an agency within the Department of Health and Human Services, announced on September 2, 2026, a 30-day public comment period regarding two significant information collection requests. This action, published in the Federal Register, fulfills requirements under the Paperwork Reduction Act of 1995, which mandates federal agencies to solicit public input on proposed or continuing data collection efforts. The notice provides an opportunity for interested parties to offer feedback on the necessity, utility, and estimated burden associated with these data collections, which play a crucial role in federal oversight of state health programs. Comments are due by October 2, 2026, and can be submitted online.

The Mandate for Public Scrutiny: Paperwork Reduction Act

The Paperwork Reduction Act of 1995 serves as a mechanism to minimize the reporting burden on the public and to ensure that government information collections are necessary and efficient. Under this statute, agencies like CMS must obtain approval from the Office of Management and Budget for any collection of information. Before submitting such requests to OMB, a 30-day notice is published in the Federal Register, allowing public and stakeholder engagement. This current notice specifically invites comments on various aspects, including the accuracy of the estimated burden, ways to enhance data quality and clarity, and the potential use of automated collection techniques.

Focus on Money Follows the Person Demonstration

The first information collection undergoing review, identified as CMS-10249 (OMB control number 0938-1053), pertains to the "Administrative Requirements for Section 6071 of the Deficit Reduction Act." This collection supports the Money Follows the Person Rebalancing Demonstration program. The MFP initiative aims to assist eligible Medicaid beneficiaries who reside in institutions to transition back into community-based settings, receiving care in their homes or other non-institutional residences.

The data gathered through this collection is multifaceted. It informs CMS project officers and other federal officials about the demonstration's operation and prepares them for potential site visits. State project directors utilize it as a program implementation manual. External stakeholders can also use the data to understand the demonstration's processes. Crucially, financial information collected is integrated into CMS's financial statements and shared with auditors to validate the agency's financial position.

Moreover, specific data files like the MFP Finders File, MFP Program Participation Data file, and MFP Services File, along with MFP Quality of Life data, are used by national evaluation contractors. This evaluation aims to assess program outcomes, particularly how participants' quality of life changes after transitioning to the community. Semi-annual progress reports submitted by grantees allow both the national evaluation contractor and CMS to monitor program implementation at the grantee level. This collection affects state, local, or tribal governments, with an estimated 41 respondents, resulting in 329 annual responses and a total annual burden of 2,706 hours.

Oversight of Medicaid Managed Care Quality

The second, and considerably larger, information collection under review is CMS-10553 (OMB control number 0938-1281), titled "Medicaid Managed Care Quality Including Supporting Regulations." This collection is fundamental to CMS's oversight responsibilities concerning state Medicaid managed care programs, which increasingly serve a substantial portion of Medicaid beneficiaries.

States are mandated to develop comprehensive quality strategies and to conduct evaluations of these strategies' effectiveness. The information derived from these documents is vital for states to monitor and assess the performance of their managed care programs. An essential component of this process involves stakeholder engagement during the development of these documents, which must also be made available for public comment. This ensures transparency and allows Medicaid beneficiaries and other stakeholders to understand a state's quality improvement goals, objectives, and progress measurement.

States are required to submit these documents to CMS for review at least every three years, or whenever significant changes are made to their quality strategies or State Medicaid programs. Furthermore, the Medicaid and CHIP Managed Care Quality Rating System (MAC QRS) requirements include public posting of quality ratings on state websites. This feature is designed to provide beneficiaries and their caregivers with an accessible, web-based interface to compare Medicaid and Children's Health Insurance Program (CHIP) managed care plans based on assigned quality ratings, fostering informed decision-making.

This collection impacts both the private sector, specifically businesses or other for-profits involved in managed care, and state, local, or tribal governments. It involves an estimated 673 respondents and 6,114 responses annually, with a substantial total annual burden of 1,444,538 hours. The significant hour burden underscores the extensive nature of quality reporting and oversight required for managed care organizations and state agencies.

Implications and Call for Comment

The ongoing review of these information collections highlights the federal government's continuous effort to balance regulatory requirements with the need for effective program oversight and evaluation. The Money Follows the Person demonstration represents a key strategy for community integration, and the data collected is critical to understanding its impact and ensuring accountability. Similarly, the extensive data collection for Medicaid managed care quality is indispensable for maintaining standards, promoting transparency, and empowering beneficiaries in a complex healthcare landscape.

The public comment period offers a vital opportunity for affected entities, including state agencies, healthcare providers, beneficiaries, and advocacy groups, to provide insights into the practical implications of these data requirements. Feedback regarding the accuracy of burden estimates, potential for streamlining collection processes, and suggestions for enhancing data utility can directly influence how these federal requirements are shaped moving forward. This process underscores the dynamic nature of federal regulation and the importance of public participation in its evolution.

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