EHRpath

Choosing the Right Path Towards
Meaningful Use

The first stage of Meaningful Use involves data collection, and can earn your practice up to $39,000 per provider.

  • Help your practice receive up to $15,000 per provider in 2013, and up to $39,000 per provider over the next 4 years
  • Learn how to advance your workflow efficiency towards full EHR integration
  • Receive guidance on forthcoming regulatory concerns and compliance

Listen to a Miraca Life Sciences expert walk you through Stage 1 of MU.

The second stage of Meaningful Use is focused on Interoperability and Connectivity.

  • Prepare for your Meaningful Use audit by ensuring adherence to CMS requirements
  • Avoid potential Medicare penalties in 2014 and successfully attest to Meaningful Use requirements
  • Prepare for the revolution in medical billing, ICD10, with guidance from our knowledgeable experts

Listen to a Miraca Life Sciences expert walk you through Stage 2 of MU.

In accordance with the HITECH Act, every applicable healthcare organization must be Meaningful Use compliant by 2015. While the complexities of transitioning to Meaningful Use may seem daunting, we have the capabilities and experience necessary to guide you along the way. EHRpath is our new comprehensive service and support system that forges a long-term partnership with healthcare professionals to decode and take action towards Meaningful Use compliance. From EHR integration to assistance in receiving nearly $40,000 in Meaningful Use incentives, we’re here to help prepare your practice for the future.

EHRpath supports your practice through pathology, technology and Meaningful Use guidance.

EHRpath builds upon our comprehensive knowledge in working with EHRs to give you confidence when integrating a new system. Our wide knowledge base allows us to help you analyze your practice's needs and find a solution that is tailored to your workflow. In addition, we organize and document the entire process to help you get the most out of the government's incentive program. It's a complete consulting solution that not only partners with your practice throughout the EHR integration process, but also provides tailored workflow solutions to help you maximize your system.

Experience You Can Use →
As a leading provider of pathology services, we work with EHR systems on a daily basis. Learn how we can put our experience to work for you.

Meaningful Use Guidance →
From CMS requirements to EHR policies and procedures, discover how EHRpath can help navigate the challenges that come with EHR system integration.

Start on the path towards full EHR integration. Contact us at 855.EHR.PATH (347.7284) or email us at MeaningfulUse@MiracaLS.com.

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The dermatopathologists are very easy to work with and will pick up the phone to discuss pathology if there are any questions.
— Susan Seidel, RN,
Office Manager,Stone Oak Dermatology, San Antonio, Texas


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Recent News


May 23, 2017

Miraca Life Sciences Again Expands Therapeutic Drug Monitoring with Addition of First Biosimilar Inflectra®

IRVING, Texas, May 23, 2017 — Miraca Life Sciences, the largest U.S. independent anatomic pathology laboratory, has further expanded its InformTx™ therapeutic drug monitoring (TDM) capabilities with the addition of testing for Inflectra® (infliximab-dyyb), which is the first biosimilar drug in the test offering. Since launching InformTx in June 2016, Miraca Life Sciences has expanded the service from four to […]

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April 18, 2017

Miraca Research News: Philips receives FDA clearance to market Philips IntelliSite Pathology Solution for primary diagnostic use in the US

Pathologists at Miraca Life Sciences contributed significantly in the development of a new product from Philips, the IntelliSite Pathology Solution. As one of four clinical study sites, Miraca Life Sciences participated in “one of the largest studies ever conducted to directly compare the use of digital pathology to optical microscopes.” At Miraca, participation in the Philips study was a project of Miraca […]

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April 11, 2017

Ten Research Projects from Miraca Life Sciences Accepted for DDW Conference

IRVING, Texas, April 12, 2017 — Ten research projects from the GI pathologists at Miraca Life Sciences, the nation’s largest independent anatomic pathology lab, have been accepted for presentation at the Digestive Disease Week® conference (DDW), which will be held May 6–9 in Chicago. DDW is the world’s largest gathering of physicians, researchers and industry in the fields of gastroenterology, […]

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March 27, 2017

Simponi® is Sixth Drug in InformTx™ Therapeutic Drug Monitoring Service from Miraca Life Sciences

IRVING, Texas, March 28, 2017 — Miraca Life Sciences, the largest U.S. independent anatomic pathology laboratory, continues to expand its InformTx™ therapeutic drug monitoring (TDM) capabilities, now testing for Simponi (golimumab) as well as patient-developed antibodies to Simponi. This is the first TDM assay available in the United States for Simponi. With this addition, Miraca Life Sciences now performs TDM […]

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November 30, 2016

Stelara® Now Available for Therapeutic Drug Monitoring from Miraca Life Sciences

IRVING, Texas, December 1, 2016 — Miraca Life Sciences, the largest U.S. independent anatomic pathology lab, has expanded its InformTx™ therapeutic drug monitoring service for drugs that treat inflammatory bowel disease (IBD) with the addition of Stelara (ustekinumab).

Miraca Life Sciences continues to perform therapeutic drug monitoring (TDM) for Remicade® (infliximab), Humira® (adalimumab), Cimzia® (Certolizumab pegol) and Entyvio® (vedolizumab). Since […]

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