In a Pharmacovigilance Computerized System it is very important to define responsabilities and workflows before the implementation of the system.

An adverse event reporting sytem must be customized according to the client's requirements. SafetyDrugs Workflow has the flexibility to be shaped according to International Rules and, at the same time, to comply to internal requirement of your company.

SafetyDrugs Workflow, in parametric manner, allows:

• to manage every phase of a Clinical Case (or Study);
• to define the time for processing every step;
• to define authorized users, the authorization level and allowed actions.

SafetyDrugs Workflow controls the correct sequence of every step in the flow, alerting the users about the deadline.