Product Overview
EvidentIQ eConsent improves trial participants experience by meeting them where they are.
It enables the improved quality and efficiency of clinical trials through insight into the patient experience, improved data quality and a fully electronic experience.
Today, study sponsors must find new ways to ensure that potential patients are fully informed, despite the multitude of information provided, traditionally on paper.
Electronic informed consent (eConsent) provides the same information, but in an electronic format that may include multimedia components such as images, audio, video, diagrams, reports and a digital signature which may aid the comprehension and consenting process with less effort.
Deployment
- Web based
- Cloud Hosted
Pricing
- Subscription
- License Fee
More Information
Simplify and speed up the consent process
Recruit your participants through a customized recruitment portal and pre-screen with questionnaires to help filter appropriate participants. Allows collection of your subject eligibility status (pending, pass, and fail) including the timestamp of when this was updated. After consent, patient data from enrolled participants can automatically be updated in the EDC system, ready for the next step.
Helping to provide the patient with the full picture
With information provided on a handwritten form the patient may not get the fullest possible account of the risks and benefits associated with the procedure they are considering. Important points may be abbreviated, illegible or missed altogether.
EvidentIQ econsent offers a wide range of eConsent design capabilities including embedded video, graphics, PowerPoint, PDF files for patients to review, consent acknowledgement checks.
Furthermore, the patient will receive the most recent versions of any associated information leaflets for the procedure and can be provided with a link to an electronic copy of the form in addition to (or in place of) a printed copy.
About the company
Leveraging more than 50 years of combined experience providing innovative and creative ways to conduct clinical trials. End-to-end eClinical Solution
Meeting increasing customer demand across clinical operations and clinical data management needs with a suite of applications within a single integrated cloud platform, including EDC, CTMS, eTMF, eCOA, coding, remote monitoring, RBM, RTSM, Payments and eFeasibility. Geographical Reach
In-country patient communities platform in North America and Western Europe (EU5) and ability to conduct studies at a broader scale (LatAM, Asia…). Regulatory expertise to support broader geographical studies.
