Articles and Blogs

Year: 2017

CMS Final Rule Establishes Significant Changes to Comprehensive Care for Joint Replacement Model

[01/18/17]

Posted on January 18, 2017 in Health Law News

Published by: Hall Render

On December 20, 2016, the Centers for Medicare & Medicaid Services (“CMS”) published a Final Rule that included several changes to the recently implemented Comprehensive Care for Joint Replacement (“CJR”) program. The CJR Model is a retrospective bundled payment program limited to lower extremity joint replacement (“LEJR”) procedures and is designed to encourage hospitals... READ MORE

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CMS Issues Final Rule for New Bundled Payment Models

[01/18/17]

Posted on January 18, 2017 in Health Law News

Published by: Hall Render

Background On December 20, 2016, the Centers for Medicare & Medicaid Services (“CMS”) published a final rule (the “Final Rule”)1 creating three new episode payment models (“EPMs”) covering services provided to Medicare beneficiaries admitted to certain Inpatient Prospective Payment System (“IPPS”) hospitals for heart attacks, coronary bypass surgery or surgical treatment of hip or... READ MORE

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CMS Finalizes New Conditions of Participation for Home Health: Part 1

[01/17/17]

Posted on January 17, 2017 in Health Law News, Long-Term Care, Home Health & Hospice

Published by: Hall Render

Review of the New Quality Assessment and Performance Improvement Condition This is the first article in a series discussing CMS’s pre-publication copy of the Final Revised Home Health Conditions of Participation (“Final CoPs”). With the release of the Final CoPs, CMS is finalizing, with only a few changes, the significant changes they proposed to... READ MORE

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Attest to 2016 Medicare Meaningful Use Program Requirements by February 28

[01/17/17]

Posted on January 17, 2017 in Health Information Technology

Published by: Hall Render

This month, the Centers for Medicare & Medicaid Services opened the registration and attestation system for the Medicare Meaningful Use Incentive Payment Program for 2016.  Eligible providers participating in the Medicare Meaningful Use Incentive Payment Program must attest to the 2016 Medicare Meaningful Use Program requirements by February 28, 2017 at 11:59 PM EST in order... READ MORE

Michigan Midwifery License Legislation Signed into Law

[01/16/17]

Posted on January 16, 2017 in Health Law News

Published by: Hall Render

On January 3, 2017, Governor Rick Snyder signed House Bill 4598 (“HB 4598”) into law. HB 4598 adds Part 171 (Midwifery) to the Public Health Code and provides new licensure requirements for the practice of midwifery in Michigan. Effective immediately, the bill establishes midwife licensure and scope of practice requirements, including: Prohibiting an individual... READ MORE

Hall Render’s This Week in Washington – January 13, 2017

[01/13/17]

Posted on January 13, 2017 in Federal Advocacy

Published by: Hall Render

Congress Completes First Step in ACA Repeal Process After a week of debate and over 100 proposed amendments in the Senate, the fiscal year 2017 budget resolution (S. Con. Res. 3) advanced to the House of Representatives on January 13, where it passed along party lines by a vote of 227 to 198. The... READ MORE

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Three Supply Chain Strategies to Impact the Bottom Line

[01/13/17]

Posted on January 13, 2017 in Health Law News

Published by: Hall Render

The supply chain continues to be the second largest and fastest growing expense for health care systems, second only to labor costs, making this an area of untapped cost savings opportunity and an area ripe for leveraging supply chain as a strategic driver of savings. Because the procurement of goods and services impacts nearly... READ MORE

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FDA Releases Final Post-Market Guidance on Medical Device Cybersecurity

[01/11/17]

Posted on January 11, 2017 in Health Law News

Published by: Hall Render

On December 27, 2016, the Food and Drug Administration (“FDA”) issued final guidance (the “Post-Market Guidance”) outlining steps that medical device manufacturers and health care systems should take to monitor, identify, understand and address cybersecurity risks once medical devices and mobile medical devices have entered the marketplace. The Post-Market Guidance follows October 2014 FDA... READ MORE

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