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Clinical Project Management

This module is available only for project managers. And since you would want to manage your projects anyway this is a mandatory module.

Manage Studies

You can create studies and manage the documentation such as IRB approvals, IB, Informed Consent and CSP. Currently only one Informed consent is supported, and if needed support for multiple consent forms (translations) can be supported. Each study should have a Study Manager.

Manage Users

New users can be created with an access expiry date. They can also be assigned to either : 1. Project manager, 2. Study Manager, 3. Research Assistant role. The plan for future is to add an investigator role.

Assign Tasks

User can be assigned specific tasks connected to a project or activity. Tasks optionally can have a delivery deadline.

SOPs

Standard Operating Procedures (SOPs) for your organization can be maintained here. The application does not support writing SOPs, and on demand clinnovo can provide sample SOPs. Also the training records for SOPs of your staff can be managed.

Audit Trial

Every activity (Except read) are recorded in the audit trial. It can sorted by date or project and filtered by user and activity type (create, delete, update, assign, acknowledge).

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