| Scope | Feature |
|---|---|
| Version | v3.17.0 |
| Release date | September 18, 2026 |
| Deployed to Confimedis Cloud | September 21, 2026 |
| Affected modules | Settings, Subjects, Forms, Documents, eConsent, Users, Notifications, Surveys |
Validation by Confimedis
Confimedis GmbH has validated this release in accordance with its quality management system and GAMP 5 before deployment, re-executing the test cases of the Operational Qualification (OQ) for the affected functions according to their risk classification. A release does not change the configuration of your study, such as forms, edit checks, roles, or users, which your Performance Qualification (PQ) covers. Where existing settings are migrated, the note says so. The Validation Package of every release, including the OQ report and a prefilled Validation Summary Report (VSR), is available on request and only needed for an initial validation or a revalidation. A test project is a copy of your study without patient data, created via CDISC ODM export and import.
Recommended action on your side
Review before useNote from Confimedis on version 3.17.0
One change is visible in running studies: In a Production project, a subject is now archived via the new Archive action before it can be deleted. Existing roles, forms, and sites are unchanged, and no PQ test item is affected. If you start using the database lock, the subject lock, the subject status, or the archiving of subjects, execute PQ 3.4 Locking and archiving permissions and PQ 4.5 Status of new subjects in a test project first, both items of the current PQ template.
Summary: Projects can now be locked for an interim analysis or once data collection is complete. Subjects carry a subject status and can be locked or archived. An eConsent can also be captured in ePRO links with the signatures of both the participant and the person providing the informed consent information.