Ethical GmbH upgrades the study designer functionality available with the eAdjudication® software platform to allow customers to independently create and configure new studies in their company dedicated workspace.
Study designer now allows trained customers to set up libraries of studies and adjudication forms and use these as templates to create and configure new studies without having to turn to Ethical. With the upgraded study designer, Ethical GmbH is expanding the eAdjudication offer to meet customer needs in different situations.
Ethical GmbH now offers two provisioning models: – The supplier-managed model, where the Ethical team creates, configures, customizes and manages the platform from set-up to archival; – And the new customer-managed model where customers purchase the software and receive training allowing them to create and configure studies with study designer. Ethical’s new customer-managed model is appropriate for organizations that use standard adjudication charter formats and have internal capabilities to administer the platform. Ethical’s supplier-managed model offers greater flexibility, adapting to any adjudication charter specification and any data and trial management architecture.
Mimmo Garibbo, Director of Ethical GmbH, says: “At Ethical GmbH, we are excited about the upgraded study designer functionality. We are now able to satisfy more eAdjudication® customer scenarios, including from organizations who prefer to independently manage their platform and to leverage the consequent economies of scale. The Ethical team will continue to offer our proven supplier-managed model for all situations where flexibility, customization and support are required.”
About eAdjudication
eAdjudication, Ethical’s electronic adjudication management system, is a cloud-based platform designed to manage clinical endpoint independent review and adjudication in a simple, effective and GxP-compliant way.
About Ethical
Founded in Basel in 2014, Ethical GmbH is an eClinical company specialized in endpoint adjudication, safety data reconciliation, Electronic Data Capture and other data management software services for clinical research with a cumulative experience of 300 international clinical trials, over 10,000 investigator sites and hundreds of thousands of patients.
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