Audience
Organizations that conduct clinical trials and studies, GPs, PCPs, Hospitals
About Track.Health
Secure and user friendly cloud-based EDC platform for managing clinical trials and studies of all sizes and complexities: ePRO, eConsent, eCOA, eSource, PROMs, PREMs, functional health assessments and participant education/engagement.
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MainEDC
Complex eClinical Solution for EDC/ERT/eCOA that significantly speeds up the start of clinical trials (up to 5 days), saves budget (up to 80% for monitoring), increases the capitalization and attractiveness of your company (noted by 89% of customers). Increases the knowledge and advancement of Data Management and Data Science professionals (noted by 96% of specialists). 94% of investigators like the usability of interfaces.
An important part of Data Management 365 policy is to have strong internal competence in Clinical Data Management and Data Science. This allows our company not only to deeper understand the challenges that Data Managers face in their work and make the MainEDC™platform better using the online feedback but also to provide the transfer of technology and best practices to our Clients.
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Trusted by CROs, sponsors, and sites across all therapeutic areas and trial phases from study startup and feasibility to post-market approval, we are industry-recognized for delivering eClinical software with intuitive interfaces and time-saving “drag and drop” configurations as well as high-touch customer engagement, onboarding, and support services.
Medrio’s innovative software, as well as the robust and flexible training and support resources we provide our customers, have earned us a 98% customer satisfaction rating.
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ShareCRF
Create, in a few hours, an eCRF that is as easy to use as a paper one, and avoid the biggest headaches in data collection in Pre-authorisation and Post-authorisation studies of your medical device. Incorporate an EDC that is highly flexible when creating the eCRF, this will allow you to meet the needs of any kind of study. Save tons of time in the management and monitoring of the study with the management and monitoring tools included in the EDC. Use a validated system with all the security guarantees that give trust to the sponsor and allow the collection of quality data. Don’t wait until the analysis phase to discover mistakes in the data or you will end up chasing down investigators to correct them. Prevent the process of creation of an eCRF from being long and complex.
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Pricing
Starting Price:
$1/participant/month
Pricing Details:
Contact us at info@pryzm.health for custom price
Free Trial:
Free Trial available.
Company Information
Pryzm Health
Founded: 2018
Australia
track.health/
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Product Details
Platforms Supported
Cloud
Training
Documentation
Live Online
Webinars
In Person
Support
Phone Support
Online
Track.Health Frequently Asked Questions
Track.Health Product Features
Clinical Trial Management
Document Management
Supported
Electronic Data Capture
Supported
Enrollment Management
Supported
Monitoring
Supported
Patient Database
Supported
Recruiting Management
Supported
Scheduling
Supported
Study Planning
Supported
21 CFR Part 11 Compliance
Not Supported
HIPAA Compliant
Not Supported
Electronic Data Capture
Audit Trail
Supported
Data Entry
Supported
Data Verification
Supported
Distributed Capture
Supported
Forms Management
Supported
Remote Capture
Supported
Study Management
Supported
CRF Tracking
Not Supported
Document Imaging
Not Supported
Document Indexing
Not Supported
