QRDA Solutions

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QRDA
needs
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QRDA Solutions
See how our
QRDA Toolkits
save time, costs and effort
 for you and your Providers

CMS submission tools
Dr. Watson QRDA
Data Verification
Data Integrity
Submission Review
CMS Audit Monitor
EHR Data Mining

 

 

                             


Is your organization ready
for the new 2016/2017 CMS Quality Reporting programs?

Increase Quality Assurance for your organization's submissions
to the new CMS QRDA compliance programs today!

Our clients have leveraged our QRDA support to expedite their 2016/2017 reporting processes
to Federal MIPS/APS/CPC+,  State Medicaid, payer and internal QA initiatives


 

 
  Minimize CMS penalties and maximize incentives
for your provider organization
with our CMS QRDA submission review tools

Optimize your CMS incentives for your providers by using our proprietary QRDA submission review tools, and minimize the penalties and workflow interruptions to your providers.  View MIPS / APS / CPC+ tools here.

 

QRDA-HISP supports
your organization

 
  
Expedite your CMS report process
with our QRDA modules

QRDA Solutions provides modular QRDA support through our secure  cloud to supply the QA report tools your organization needs.

When you simply your process by using our bolt-on QRDA toolkit, your organization can create submissions for CMS EH and EP organizations  and State QA initiatives by exporting patient data from your EHR.

 
QRDA services
Improve submissions

Lower costs

CMS & ONC compliance

 
   We lower your CMS reporting costs

Registries and EHR vendors charge a premium for QRDA report services; many report processes can be performed by your IT staff. 

Does your organization need to improve the QRDA submission while containing QRDA reporting costs?

Our QRDA toolkit eliminates the CMS and QRDA related charges for EHR modules or retain expensive registry consultants, who are simply translating your exported patient data.

 

 

   

Our process leverages your current technology.

Problem: Your current EHR version does not fulfill CMS requirements, while your EHR vendor requires costly upgrades that may break or change other EHR functions.
 

Solution: Our procedures leverage your current technology to optimize CMS measure selection for all applicable CMS reporting channels achieve 2016 & 2017 CMS submission compliance.


Benefit: IT requirements are minimized for 2016 & 2017 CMS requirements.
 

 

   
We leverage your current IT resources

Solution: Your IT staff knows how to extract reports from your EHR. 
Why pay an expensive registry to duplicate these efforts?

Benefit: Staff resources are used instead of hiring an expensive CMS Registry consultant.
 

 

 

   

 Our processes fulfill CMS QRDA report requirements
and minimize workflow impact 

Problem: New CMS 2015 mandates triple the payload required of CMS submissions.


Solution: Our procedures streamline CMS report logistics to optimize all stages of QCDR submission preparation.


Benefit: Your practice's CMS payment adjustments are optimized with minimum workflow interruptions.
 

 

   
Scheduled automated validation of your CMS submissions

Solution: Our Submission Auditor uses proven data validation and scrubbing processes where errors are identified at all stages of the CMS / QRDA submission generation process.  Our CMS Measure Map Compiler extracts strategic data from your EHR, PM, and CMS billing records to optimize CMS measure selection and evaluating CMS quality report channels.


Benefit: Validated CMS reports save time and resources for your staff.
 

 

CMS QCDR
Compliance
 Audit

  Passed

   
 Our Dashboard manages the QCDR/QRDA submission process

Solution: Our dashboard manages the generation, review, and transmittal of complex QRDA documents sourced by multiple EP electronic record systems by leveraging proven financial audit trail technologies. 

Benefit: Our dashboard  enables efficient management of the CMS submission process.
 

 
QRDA
Quality
Reporting
Document
Architecture


CMS
2015 QRDA specs

 
cc: To all Healthcare Providers and HIT Vendors:


2016 and 2017 CMS rules change your submissions...

CMS mandates QRDA compliance

Is your organization ready for QRDA?

CMS 2016 rules mandate Quality Report Document Architecture (QRDA) compliance for quality submissions from CMS healthcare delivery systems.  

 

When is your first QRDA submission due?

 

We expedite your capacity to generate, validate and review QRDA submissions by having tested solutions that extends life cycle of your existing systems.  Read more... 

 

 
  Is your organization installing redundant Quality Assurance (QA)
systems? 

After installing multiple QA report subsystems that are probably redundant, many Healthcare organizations are suffering these symptoms:  
 

- Exploding CMS quality reporting costs - MIPS/APS/CPC+/QRDA/VBM...

- Escalating maintenance upgrades

- Lack of CMS compliance - Missed submission dates
 

Multiple QA installations cause these problems when vendors can not meet inevitable Federal and State regulatory timetables for the innumerable changes in interrelated submission requirements. 

 

Our QRDA toolkit minimize the resources, complexity and time required by centralizing Federal (CMS/CDC) and State QA functions Read more . . .

 

 
   QCDR has already used our QRDA report subsystems

CMS designated the Qualified Clinical Data Registry as the CMS report channel to test QRDA report processes.

 

Healthcare organizations and QCDR's have discovered that the increased CMS submission payload increases the development and support costs for QA report subsystems can dramatically escalate if universal QRDA subsystems modules are not implemented.

 

We have spearheaded the outsourcing of QRDA compilers and quality report applications.  Our system components encapsulate regulatory updates; This enhances the value of QRDA to your organization.

Our concise integration of QRDA modules significantly reduces the time and costs of development, maintenance and future support.   Read more . . .

 
     
QRDA review
Checklist

Eligible measure list
Data integrity
Vetting

 
  Our QRDA review tools minimize regulatory exposure

We provide the tools necessary to review QRDA reports before they are transmitted to regulatory agencies.

Our QCDR-HISP Hybrid Cloud insures that your organization complies with the CMS mandated CMS record integration processes.

 
CMS MU2
Mandates

Expanded measure list
VBM support
Data integrity
Vetting

 
   Our
QRDA modules EHRs comply with MU2

The myriad of MU2 EHR mandates for CMS Quality Submissions increase development costs and time to market.   2014 has already initiated another cycle of CMS CMS rule updates which will propagate into code changes; CMS functions can be simplified with outsourced functions by using a systematized approach dedicated to MU2 CMS compliance. 

Our QCDR-HISP Hybrid Cloud insure that your EHR complies with the  CMS mandated MU2 reporting requirements.

 
QRDA/CMS
Audit support


CMS & HIPAA compliance

ISO-9000 documentation
 
 
   We document and secure your QRDA/CMS audit trails

Documentation is central to effectively managing IT resources that respond to Federal mandated report programs; tracking regulatory changes can grow into expensive and time consuming upgrades.   Outsourcing various QRDA & CMS components streamline these processes. 

Our documentation and implementation procedures insure that you maintain schedule and cost control over the CMS submission process.

 

 
  Our QRDA processes plan for MIPS regulatory changes

Your organization can reduce regulatory exposure by embracing modular solutions using our QCDR-HISP Hybrid Cloud.  Following regulatory trends is embedded in our system design processes. 

Documentation is central to effectively managing IT resources that respond to Federal mandated report programs; tracking regulatory changes can grow into expensive and time consuming upgrades.   Outsourcing various QRDA & CMS components streamline these processes. 

Our documentation and implementation procedures insure that you maintain schedule and cost control over the QCDR submission process.

CMS and many state health agencies currently require Clinical Quality Reports (CQR) to be submitted using the Quality Reporting Document Architecture (QRDA). 

The CMS audit process for QCDRs requires the ability to be able to trace associated CMS and medical records while maintaining HIPAA compliance.  Automating the CMS compliance processes usually involves the complex integration of CMS-1500/837P claim records.

 


We save your organization time, effort and resources to comply with QRDA standards.
 

 
In order to fulfill CMS QRDA quality reporting requirements,
CMSGATEWAYS.COM compiles and validates incoming data from many sources as well as the CMS submissions with our Report Generation Engine by using our efficient data-mining processes for provider HIT databases and EHRs.
 

CMSGATEWAYS.COM  provides a support services to fully leverage your existing registry IT to enable your organization to orchestrate a tiered, efficient QRDA submission process.  More...

 

QRDA - QRDA roundtable at ONC 2014 Meeting

Summary report available for @ 2014 ONC Annual meeting Details here

 

 

  For more information, contact us at clientservices@cmsgateways.com

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

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Last modified: Monday December 05, 2016.