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QCDR-HISP

Qualified Clinical Data Registry - Health Information Service Provider

Minimizing the costs of regulatory transition


 

 

MACRA is a game changer for physicians, payers and QCDRs. 

Rules are evolving as implementation dates approach. 

QCDR-HISP works with QCDRs to rapidly respond to reporting requirements
   by helping you re-tool your systems and maximize existing capacity. 
 

MACRA

Our Goal: Minimize resource requirements for CMS regulatory transitions Minimize the resource requirements for CMS regulatory transitions
  • Problem: Excessive costs to achieve MACRA compliance

  • Goal: Meet MACRA objectives with a staged transition that minimizes your organization's resource allocation

  • Solution: We provide valuable QCDR functions that expedite compliance with both CMS and
    MULTIPLE state Medicaid mandates

    • Our catalog of CMS and State Medicaid report functions include:

      HCC Risk Stratification
      Dual Eligibility Scoring Coefficient
      State Medicaid Quality Submission Translation
      Cross Specialty and Cross Setting QI

  • To expedite your 2018 MACRA compliance TODAY:

    • Receive hyperlinks to our 2018 MACRA toolkit by joining our users group HERE

    • You'll receive timely notification when MACRA coverage expands


 

MANAGING
REGULATORY
TRANSISTIONS

 

 

MACRA Public Health reporting toolkit MACRA Public Health Reporting Toolkit  
  • MACRA objective: Integrate multi-state Public Health reporting systems

  • Problem: Fragmentation - Each state has a different support model for Public Health reporting

  • Goal: Unify the Public Health Reporting interface QCDRs, EHRs, EPs, state agencies, and CMS

  • Solution: Create a MACRA compliant Multi-state Public Health Reporting Toolkit

    • Establish a tiered development model to align with MACRA objectives

    • Create an index for each state's reporting mechanism for Public Health reporting

      • Identify alignment of state regulations with MACRA

    • Develop, support and maintain an extensible Public Reporting System

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MACRA QI components MACRA QI components  
  • MACRA transition: Descriptive to Prescriptive.

    • Clinical relevance toolkit

      • Conversion from Administrative (HEDIS) to Clinical quality tools (EHR)

    • De-fragmentation processes

    • Individual alignment of MACRA components with resource allocation priorities

    • Using vetted solutions to expedite development

 

Achieve CMS Compliance.

On time.

Future list of MACRA issues Future list of MACRA issues to be extended here
  • Future MACRA component support processes will be added to this web site.

  • For future reference, bookmark this page.  Revisit this site for updates.

  • Send a request for coverage of a particular MACRA component HERE

  • Receive timely notifications by joining our MACRA-QCDR support group HERE

 


 CMS Gateways
is committed to helping our nation achieve better and affordable care, and improving the overall health of Americans by providing efficient solutions that compile, review and transmit accurate MACRA submissions to CMS.  

"Providers require CMS Compliant Report systems that are cost effective
to stay competitive in the ever changing regulatory environment"

Choosing to take advantage of our integrated CMS submission process saves your organization time, effort and resources.

Specifically,  CMS Gateways  has engineered and implemented the following QCDR solutions:

  CMS Gateways  delivers solutions for corporate and registry clients that that are cost effective to stay competitive in the ever changing regulatory environment.

 

 CMS Gateways  provides a portfolio of quality report submission services to achieve these goals:

        - Analyze, design and administer staged procedures inherent in CMS reporting processes

        - Identify, localize and coordinate EHR vendor sensitive issues

        - Collaborative seminars and roundtables to facilitate implementation solutions

        - Exploit Common Point Access Methods with thorough data validation and integration

In order to fulfill CMS requirements for Qualified Clinical Data Registry (QCDR),
 CMS Gateways compiles and validates CMS submissions with our Submission Generation Engine
by using our efficient Data-Mining processes for patient experience databases and provider EHRs.
 CMS Gateways   provides a secure, reliable QCDR Cloud to fully leverage your existing registry IT to enable your organization to orchestrate a tiered, efficient QCDR submission process.  More...
 

QCDR roundtable progress at ONC 2014 Meeting Details here


  For more information, contact us at clientservices@qcdr-hisp.org

QCDR-HISP = Qualified Clinical Data Registry - Health Information Service Provider

QRDA Submission Template, QRDA Submission Toolkit, QRDA Audit Tool, QRDA Validator, QRDA Aggregator and NwHIN Sleuth are trademarks of CMS Gateways, LLC
All other products mentioned are registered trademarks or trademarks of their respective companies.

Questions or problems regarding technical problems for this web site should be directed to
clientservices@qcdr-hisp.org
Copyright © 2016 CMS Gateways, LLC. All rights reserved.
Last modified: Friday May 06, 2016.