Avia Logo

Compare Products


Jump to:
Categories
Solutions
Description
Compatibility Level
Clients
Use cases
EHR integrations
Client types
Differentiators
Keywords
Media
Company details
Jump to:
Categories
Solutions
Description
Compatibility Level
Clients
Use cases
EHR integrations
Client types
Differentiators
Keywords
Media
Company details
YouScript
YouScript

0 review

 GenoAct
GenoAct

0 review

Categories

Solutions

Description

Product Description:
Our clinical decision support tool synthesizes the evidence impacting drug response, including pharmacogenomic testing, to support doctors and pharmacists in making faster, more proactive decisions at the point of care. YouScript is the only clinical decision support system validated in multiple clinical and real world studied system. In a recent study, utilization of YouScript and pharmacogenomic testing revealed 52% reduction in readmissions and 42% reduction in ED visits. And we’re successfully integrated into the clinical workflow of Epic, Cerner, Allscripts, and Telus Health. Equally important is that our team includes pioneers in genetics, medicine, technology, and genetic counseling, and is trusted by experts to provide the most comprehensive, reliable genetic screening, technology, and support available. In pursuit of our mission, we aim to be a trusted partner to value-based healthcare organizations, providers, and payers who want to lower the barriers of precision medicine through transforming clinical decisions through genomics.
About Invitae:
Invitae is a genetics information company whose mission is to bring genetic information into routine medical practice to improve the quality of healthcare for billions of people. Specializing in genetic diagnostics for hereditary disorders, diagnostics, pharmacogenomics, and digital health tools, Invitae is aggregating the world’s genetic tests and technologies into a single service with better quality, faster turnaround time, and a lower price than most single-gene diagnostic tests today. What’s our plan? It takes three steps: --Make genetic testing more affordable and accessible than ever before. --Build a secure and trusted genome management infrastructure. --Design a new global community for sharing genetic information to advance science and medicine. Today, we are reinventing genetic testing by lowering the barriers for clinicians and patients to obtain diagnostic genetic information. Together we can improve healthcare for billions of people. Invitae is a leader in advanced medical genetics. Our company was founded with a singular mission: to make genetic information affordable and accessible to everyone who can benefit from it. The Invitae team includes pioneers in genetics, medicine, technology, and genetic counseling, and is trusted by experts to provide the most comprehensive, reliable genetic screening and support available. Through all stages of life and all areas of medicine, when the question is genetics, the answer is Invitae.
Product Description:
ActX is a genomic decision support service that is tightly integrated within the EHR. With ActX implemented, every time a prescription order is written in the routine medication order workflow, it will be checked for drug-genome interactions and the prescriber alerted as needed. Provider friendly, and CAP accredited initial results will be generated and returned to the provider in the clinical inbasket. A dynamic and up-to-date Genomic Profile for each patient will be available in their chart. Patient genetic data can be imported from any clinically valid source. The knowledgebase content is easily customizable and includes content for pharmacogenomics, actionable genetic risks, and carrier statuses.
About ActX, Inc.:

ActX helps physicians make better decisions about medical treatment, using patients’ genetic information. ActX uses its GenoACT℠ clinical decision support program to analyze a patient’s genetic information and alert physicians in real time through their existing workflow tool, the electronic health record, about drug-genome interactions, actionable hereditary risks and carrier status

Compatibility level

Select which hospital or health system you work at and see a personalized compatibility level.

Clients

Select which hospital or health system you work at and see the client list

Use Cases

Description:

None provided

Pediatric use cases:

None provided

Users:

None provided

Description:
  • Yale Generations project
  • NorthShore University Health System DNA 10k Program


Pediatric use cases:

Pharmacogenomics and actionable genetic risks.

Users:
  • Pharmacy
  • Lab
  • IT
  • All clinicians (including most specialties)
  • Genetics
  • Genetic Counselors

EHR Integrations

Integrations:

None provided

EMR Integration & Relevant Hardware:

None provided

EMRs Supported:

None provided

Hardware Compatibility:

None provided

Integrations:

Acute care EMR, Ambulatory EMR, Patient portal, Pop health platform, Behavioral health, Community based organizations

EMR Integration & Relevant Hardware:

Required

EMRs Supported:

Epic, Cerner, Allscripts, eClinicalWorks, Athenahealth

Hardware Compatibility:

Not applicable

Client Types

None provided

Differentiators

Differentiators vs EHR Functionality:

None provided

Differentiators vs Competitors:

None provided

Differentiators vs EHR Functionality:

Please reach out to ActX for more information.

Differentiators vs Competitors:

Please reach out to ActX for more information.

Keywords

Images

No images provided

No images provided

Videos

No videos provided

No videos provided

Downloads

No content provided

Alternatives

Company Details

Founded in 2010

Founded in 2012

team illustration
Share your product comparison with your collegues.

Need help narrowing down products?

Add more criteria to see your compatibility level for every vendor. It only takes a few minutes, just create a free account to get started.
back to top