Department of Health and Human Services June 3, 2013 – Federal Register Recent Federal Regulation Documents

Office of the Director, National Institutes of Health; Notice of Meeting
Document Number: 2013-13180
Type: Notice
Date: 2013-06-03
Agency: Department of Health and Human Services, National Institutes of Health
Medicaid Program; Increased Federal Medical Assistance Percentage Changes Under the Affordable Care Act of 2010; Correction
Document Number: 2013-13151
Type: Rule
Date: 2013-06-03
Agency: Centers for Medicare & Medicaid Services, Department of Health and Human Services
This document corrects a typographical error that appeared in the final rule published in the April 2, 2013 Federal Register entitled ``Medicaid Program; Increased Federal Medical Assistance Percentage Changes Under the Affordable Care Act of 2010.''
Agency Information Collection Activities; Proposed Collection; Comment Request: Generic Clearance for the Collection of Qualitative Feedback on Agency Service Delivery, National Institute of Neurological Disorders and Stroke (NINDS)
Document Number: 2013-13074
Type: Notice
Date: 2013-06-03
Agency: Department of Health and Human Services, National Institutes of Health
As part of a Federal Government-wide effort to streamline the process to seek feedback from the public on service delivery, the National Institute of Neurological Disorders (NINDS) has submitted a Generic Information Collection Request (Generic ICR): ``Generic Clearance for the Collection of Qualitative Feedback on Agency Service Delivery'' to OMB for approval under the Paperwork Reduction Act (PRA) (44 U.S.C. 3501 et. seq.).
NIOSH List of Antineoplastic and Other Hazardous Drugs in Healthcare Settings 2014: Proposed Additions and Deletions to the NIOSH Hazardous Drug List
Document Number: 2013-13043
Type: Notice
Date: 2013-06-03
Agency: Centers for Disease Control and Prevention, Department of Health and Human Services
The National Institute for Occupational Safety and Health (NIOSH) of the Centers for Disease Control and Prevention (CDC) announces the availability of the following draft document for public comment entitled ``NIOSH List of Antineoplastic and Other Hazardous Drugs in Healthcare Settings 2014: Proposed Additions and Deletions to the NIOSH Hazardous Drug List.'' The document and instructions for submitting comments can be found at https://www.regulations.gov. This guidance document does not have the force and effect of law. Public Comment Period: Comments must be received by August 2, 2013.
Proposed Data Collections Submitted for Public Comment and Recommendations
Document Number: 2013-13039
Type: Notice
Date: 2013-06-03
Agency: Centers for Disease Control and Prevention, Department of Health and Human Services
Agency Forms Undergoing Paperwork Reduction Act Review
Document Number: 2013-13038
Type: Notice
Date: 2013-06-03
Agency: Centers for Disease Control and Prevention, Department of Health and Human Services
Announcement of Requirements and Registration for “Continuity of Care and Follow-Up App Challenge”
Document Number: 2013-13018
Type: Notice
Date: 2013-06-03
Agency: Department of Health and Human Services
The ``Continuity of Care and Follow-Up App Challenge'' challenges individuals and organizations with the development of an application for a mobile handheld device that will provide continuity of care and follow-up care linkages for a person at risk for suicide who was discharged from an inpatient unit or emergency department. Proposed activities can include but are not limited to: live chatting via the National Suicide Prevention Lifeline Web site, safety planning, SMS [you need to spell this out] functionality, scheduling functionality and appointment reminders, and mapping/transportation functionality showing locations of health care resources. At a minimum, entrants must include safety planning and utilize two resources to provide users with access to services through the crisis centers within the National Suicide Prevention Lifeline and the SAMHSA treatment locator. SAMHSA is not looking for an application that simply connects a user to a crisis line via a single button, as functionality is found in a number of other suicide prevention applications. Innovation is highly encouraged. The statutory authority for this challenge competition is Section 105 of the America COMPETES Reauthorization Act of 2010 (Pub. L. 111- 358), and Title V, Section 501 of the Public Health Service Act (42 U.S.C. 290aa).
Agency Forms Undergoing Paperwork Reduction Act Review
Document Number: 2013-12978
Type: Notice
Date: 2013-06-03
Agency: Centers for Disease Control and Prevention, Department of Health and Human Services
Prospective Grant of Co-Exclusive Licenses: Multi-Focal Structured Illumination Microscopy Systems and Methods
Document Number: 2013-12967
Type: Notice
Date: 2013-06-03
Agency: Department of Health and Human Services, National Institutes of Health
This is notice, in accordance with 35 U.S.C. 209(c)(1) and 37 CFR 404.7(a)(1)(i), that the National Institutes of Health (NIH), Department of Health and Human Services, is contemplating the grant of co-exclusive worldwide licenses to practice the inventions embodied in: E-005-2012/0, /1, /2; U.S. Provisional Patent Application 61/602,139 filed February 23, 2012, U.S. Provisional Patent Application 61/732,460 filed December 3, 2012, and International Patent Application PCT/ US2013/27413 filed February 22, 2013 to Andor Technology PLC. having a principle place of business in Belfast, Northern Ireland, and to Vutara, Inc. having a principle place of business in Salt Lake City, Utah. The United States of America is an assignee to the patent rights of these inventions. The contemplated co-exclusive license may be in a field of use directed to microscopy devices and systems.
Incentives for Nondiscriminatory Wellness Programs in Group Health Plans
Document Number: 2013-12916
Type: Rule
Date: 2013-06-03
Agency: Employee Benefits Security Administration, Department of Labor, Department of Health and Human Services, Internal Revenue Service, Department of Treasury, Department of the Treasury
This document contains final regulations, consistent with the Affordable Care Act, regarding nondiscriminatory wellness programs in group health coverage. Specifically, these final regulations increase the maximum permissible reward under a health-contingent wellness program offered in connection with a group health plan (and any related health insurance coverage) from 20 percent to 30 percent of the cost of coverage. The final regulations further increase the maximum permissible reward to 50 percent for wellness programs designed to prevent or reduce tobacco use. These regulations also include other clarifications regarding the reasonable design of health-contingent wellness programs and the reasonable alternatives they must offer in order to avoid prohibited discrimination.
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