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What we do |
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QRDA-HISP supports
your EHR and PM |
Our QRDA modules expedite your
PQRS report process
QCDR-HISP provides modular QRDA/PQRS
support through our secure cloud to supply the report tools
your organization needs.
Using our toolkit, your
organization can create QRDA reports by exporting patient data from
your EHR.
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QRDA services
Second source
Lower costs
CMS & HIPAA compliance
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We lower your PQRS reporting costs
Registries and EHR vendors
charge a premium for QRDA report services; many report processes can
be performed by your IT staff.
Your organization needs to
contain QRDA/PQRS reporting costs.
Our QRDA toolkit eliminates the
QRDA charges for EHR modules or retain expensive registry
consultants, who are simply translating your exported patient data.
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Maximize PQRS return for your
providers
Maximize the CMS incentives for
your providers by using our proprietary QRDA 3 report review tools,
and minimize the penalties and workflow interruptions to your providers.
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QRDA
review
Checklist
Eligible measure list
Data integrity
Vetting
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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 PQRS record integration processes.
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CMS
MU2
Mandates
Expanded measure list
VBM support
Data integrity
Vetting
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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
PQRS rule updates which will propagate into code changes; PQRS
functions can be simplified with outsourced functions by using a
systematized approach dedicated to MU2 PQRS compliance.
Our QCDR-HISP Hybrid Cloud
insure that your EHR complies with the CMS mandated MU2
reporting requirements.
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QRDA/PQRS
Audit support
CMS & HIPAA compliance
ISO-9000 documentation
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We document and secure your QRDA/PQRS 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 & PQRS components streamline these
processes.
Our documentation and implementation procedures
insure that you maintain schedule and cost control over the PQRS
submission process.
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Our QRDA processes plan for MU 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 & PQRS 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.
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Patient Adherence Metrics
Patient Adherence Metrics
embrace automatic reminders to encourage adherence to regimens,
preventive care and followup visits, all of which leads to
decreased hospitalizations.
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QCDR-HISP Hybrid Cloud Support for
PQRS submissions
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For
QCDRs,
the challenge is how to assist your providers
to improve healthcare delivery services
by meeting the CMS report mandates
that address these issues
and minimize the impact
on all participants in the CMS report process.
QCDR-HISP.ORG
has a full portfolio
of quality report submission services to achieve
these goals.
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Our Integrated CMS submission process
saves your organization time, effort and resources |
In order
to fulfill CMS requirements for Qualified Clinical Data Registry (QCDR),
QCDR-HISP.ORG
compiles and validates incoming data from many sources as well as the CMS submissions with our Report Generation Engine
by using our efficient datamining processes for
patient experience databases and
provider EHRs.
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QCDR-HISP.ORG
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 progress at ONC 2014 Meeting Summary report available for
QCDR roundtable @ 2014 ONC Annual meeting Details
here |
