February 6–9, 2023
SCOPE – Summit for Clinical Ops Executives
FISMA 800-53 Rev4 Moderate, with NIH ATO, FDA Part 11 Compliant
> VIEW OUR FULL DATA CAPABILITIES
Want to explore how MyDataHelps™ can power your next clinical trial, research or health project?
Create an account with free access up to 100 participants.
2M
MyDataHelps™ participants
55K
EHRs connected to MDH
25M
COVID tests distributed
200K
Wearable / devices connected
17M
Surveys delivered
Create a free account and start to build out your project with NO CODING required.
Choose from the survey library or create your own clinical outcome assessments (eCOA: ePROs, clinROs, perfOs) and set custom delivery schedules. Enable wearable/device, EHR, and claims data collection.
Easily screen and reach eligible participants wherever they are with multi-modal outreach (email, SMS, QR code, in-person) and collect eConsent with eSignatures.
Schedule custom adherence notifications (SMS, push, email), provide rewards like eGiftCards, deliver educational resources, and return results to participants on dashboards.
Use remote patient/participant monitoring and automated, individualized digital interventions, including just-in-time adaptive interventions, to influence participant behavior and identify risks.
Query participant data or have it delivered to you—MyDataHelps™ exports your data to your SFTP server or S3 bucket in CSV, JSON, or Parquet format.
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> DISCOVER OUR FULL DATA CAPABILITIES![]() |
Surveys
Notifications
Device data
Participant information
EHR connections
Data is securely stored in the HIPAA compliant, Meaningful Use Certified EDC HIEBus™ platform, and is then exported to researchers in an easy-to-use format, allowing scientists to focus on science.
The MyDataHelps™ platform complies with the security and privacy controls defined by NIST 800-53 Rev. 4 at the FISMA Moderate baseline. We regularly undergo external formal assessments by a FedRAMP-accredited Third Party Assessment Organization (3PAO). Our platform has been granted an Authorization to Operate (ATO) by the National Institutes of Health (NIH) and is FDA Part 11 Compliant.