Centers for Medicare & Medicaid Services: Information Collection for Machine Readable Data for Provider Network, Prescription Formulary Content
The notice was issued by
Director, Paperwork Reduction Staff,
DATES: Comments must be received by
FOR FURTHER INFORMATION CONTACT:
* * *
The
Under the Paperwork Reduction Act of 1995 (the PRA), federal agencies are required to publish notice in the
Interested persons are invited to send comments regarding our burden estimates or any other aspect of this collection of information, including the necessity and utility of the proposed information collection for the proper performance of the agency's functions, the accuracy of the estimated burden, ways to enhance the quality, utility, and clarity of the information to be collected, and the use of automated collection techniques or other forms of information technology to minimize the information collection burden.
SUPPLEMENTARY INFORMATION:
Contents
This notice sets out a summary of the use and burden associated with the following information collections. More detailed information can be found in each collection's supporting statement and associated materials (see ADDRESSES).
CMS-10558Information Collection for Machine Readable Data for Provider Network and Prescription Formulary Content for FFM QHPs
CMS-10393Beneficiary and Family Centered Data Collection
Under the PRA (44 U.S.C. 3501-3520), federal agencies must obtain approval from the
Information Collection
1. Type of Information Collection Request: Extension of a currently approved collection; Title of Information Collection: Information Collection for Machine Readable Data for Provider Network and Prescription Formulary Content for FFM QHPs; Use: Under 45 CFR 156.122(d)(1)(2), 156.230(b), and 156.230(c), and in the final rule, Patient Protection and Affordable Care Act; HHS Notice of Benefit and Payment Parameters for 2018 (CMS-9934-F), standards for qualified health plan (QHP) issuers (including Small Business Health Options Program (SHOP) issuers and stand-alone dental plans (SADP) issuers) are established for the submission of provider and formulary data in a machine-readable format to the
2. Type of Information Collection Request: Extension of a previously approved collection; Title of Information Collection: Beneficiary and Family Centered Data Collection; Use: To ensure the QIOs are effectively meeting their goals, CMS collects information about beneficiary experience receiving support from the QIOs. The information collection uses both qualitative and quantitative strategies to ensure CMS and the QIOs understand beneficiary experiences through all interactions with the QIO including initial contact, interim interactions, and case closure. Information collection instruments are tailored to reflect the steps in each type of process, as well as the average time it takes to complete each process. The information collection will:
* Allow beneficiaries to directly provide feedback about the services they receive under the QIO program;
* Provide quality improvement data for QIOs to improve the quality of service delivered to Medicare beneficiaries; and
* Provide evaluation metrics for CMS to use in assessing performance of QIO contractors.
To achieve the above goals, information collection will include: Experience survey, direct follow-up and general feedback web survey. Form Number: CMS-10393 (OMB control number: 0938-1177); Frequency: Once; Affected Public: Individuals or households; Number of Respondents: 9,100; Number of Responses: 9,100; Total Annual Hours: 2,191. (For policy questions regarding this collection, contact
Director, Paperwork Reduction Staff,
[FR Doc. 2020-15541 Filed 7-16-20;
BILLING CODE 4120-01-P
The document is published in the
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