EHR to EDC: New software solution ‘ingests’ output data as solution to interoperability

By Melissa Fassbender

- Last updated on GMT

(Image: iStock/shansekala)
(Image: iStock/shansekala)

Related tags Electronic health record Clinical research Clinical trial

Crucial Data Solutions, Inc. and its strategic partner Zircon Technologies have teamed up to release a “first-of-its-kind” software solution developed to accelerate the clinical trials process.

Crucial Data Solutions and Zircon Technologies joined together with the common goal to lower the cost and duration of clinical research​,” said Carley Allison, director of marketing, Crucial Data Solutions

When asked how AccelEDC is different from similar solutions, Allison told us to the company’s knowledge, the technology is the first of its kind and “there are currently no solutions with similar capabilities​.”

Allison explained AccelEDC addresses the electronic health record (EHR) to electronic data capture (EDC) interoperability problem from a different angle: “instead of attempting to integrate with an EHR system, this platform simply ingests EHR output data, such as doctor's notes and PDF documents through the utilization of a lightweight API​.” 

According to the companies, the technology was developed in response to the challenge of source data verification.

The platform enables clinical research coordinators (CRCs) to export PDF files containing data, text notes, and adverse events from an EHR system. The data is anonymized with the Zircon Technologies’ AccelEDC desktop app before it is uploaded to the Crucial Data Solutions’ EDC system, Clinical Studio.

The solution also adheres to 21 CFR Part 11​ and HIPAA regulations.

The California-based contract research organization (CRO), Oncotherapeutics, is implementing AccelEDC at one of its sites in a pilot study in early 2018.

Related news

Show more

Related products

show more

Drug Solubility and the Need for Speed

Drug Solubility and the Need for Speed

Lonza Small Molecules | 28-Mar-2023 | Technical / White Paper

A growing number of new chemical entities are highly insoluble, leading to problems with bioavailability. Drug manufacturers therefore have to find ways...

Are You Prepared to Meet the New FDA Guidelines?

Are You Prepared to Meet the New FDA Guidelines?

Elligo Health Research® | 23-Mar-2023 | Insight Guide

On April 15, 2022, the U.S. Food and Drug Administration issued a new draft guidance to clinical research sponsors on creating a plan to enroll more participants...

ODM and CDASH in CRF design

ODM and CDASH in CRF design

Formedix | 10-Mar-2023 | Technical / White Paper

The lesser-known Operational Data Model (ODM) standard is often overlooked as it's not required by any regulators. So, why should you be interested...

4 Warning Signs Your Research Site Is in Trouble

4 Warning Signs Your Research Site Is in Trouble

Elligo Health Research® | 10-Mar-2023 | Insight Guide

You want your clinical research practice to be a success for your business and your patients, but how can you tell if it’s in trouble? Read this article...

Related suppliers

Follow us

Products

View more

Webinars