Chronisia has arrived: plan, monitor and comply with regulatory deadlines
Chronisia is the software solution for pharmaceutical companies that automates the management of deadlines related to PSURs, RMPs, MA renewals and other regulatory obligations.
Three core functions designed to make processes clearer, more collaborative and fully traceable.
Calculate deadlines
Enter the relevant data, select the regulatory authority and define the applicable frequency rules: Chronisia automatically determines deadlines for each product and territory.
Monitor and collaborate
Assign tasks to team members, receive automated notifications and track the status of each deadline in real time.
Ensure compliance
Maintain full traceability of all activities, with a structured, audit-ready history.
With Chronisia, every deadline has its place: from calculation to compliance, everything is under control.
SafetyDrugs and Chronisia: a coordinated approach to pharmacovigilance processes
Two solutions, one shared vision: reducing regulatory risk.
SafetyDrugs manages pharmacovigilance data and operational workflows.
Chronisia plans and monitors related regulatory activities, such as PSURs, RMPs and marketing authorisation renewals.
Together, they form a comprehensive ecosystem to:
- reduce the risk of errors and delays;
- improve coordination between PV and RA teams;
- ensure continuous and well-documented compliance.
Frequently asked questions about Chronisia
Can I use Chronisia without SafetyDrugs?
Yes. Chronisia is a standalone solution, designed to support the management of regulatory deadlines independently of SafetyDrugs.
For companies already using SafetyDrugs, Chronisia represents a natural complement to better coordinate regulatory activities linked to pharmacovigilance.
Does Chronisia replace Excel or work alongside it?
Yes. Chronisia is a standalone solution, designed to support the management of regulatory deadlines independently of SafetyDrugs.
For companies already using SafetyDrugs, Chronisia represents a natural complement to better coordinate regulatory activities linked to pharmacovigilance.
How complex is it to get started?
Chronisia has been designed to be intuitive and easy to adopt by pharmacovigilance and regulatory affairs teams.
The initial setup allows products, rules and deadlines to be configured clearly, reducing operational complexity and making the system usable from the very first stages.