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ServiceUpdated on 3 August 2026

eConsent Tool for Non-Interventional Studies

Executive Assistant ǀ Client Manager ǀ Medical Writer at M.A.R.C.O. GmbH & Co. KG - Institute for Clinical Research and Statistics

Düsseldorf, Germany

About

The eConsent functionality enables study participants to review and electronically sign the informed consent within the eCRF environment. It provides a secure digital workflow, enhances the participant experience, streamlines site operations, and supports regulatory compliance throughout the informed consent process.

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