The only Global Regulatory Intelligence System built by pharmacovigilance experts
ikyzen is a regulatory intelligence collection tool dedicated to improving efficiency in pharmacovigilance and clinical drug safety.
The ikyzen team is dedicated to excellence in service delivery within pharmacovigilance.
We developed ikyzen to solve a common problem across pharmacovigilance departments. A problem not unique to any one PV department, but an Industry-wide challenge.
The collection, assimilation and upkeep of constantly evolving regulatory requirements across the globe is extraordinarily time-consuming and difficult. Yet this information forms the foundation of compliance and patient safety.
The ikyzen system complements pharmacovigilance and regulatory activities across the Industry as the single resource of regulatory intelligence information. Introducing ikyzen to the Industry immediately relieves an immense and cumbersome burden associated with independent regulatory intelligence collection processes.
ikyzen brings a fresh approach to the management of pharmacovigilance and drug safety operations. With ikyzen, we look forward to an Industry that is no longer burdened by the challenges of regulatory intelligence collection; which in turn can confidently and effortlessly meet the demands placed upon it by Regulatory Authorities and Agencies around the world.
Global Requirements at your fingertips
Downloadable, targeted regulatory requirements.
Ready-made information for immediate use within your projects
No additional review or assimilation required by your teams.
Access historical changes or updates.
Receive monthly or quarterly update reports per country.
A global regulatory intelligence system built by vigilance experts for vigilance departments
The only regulatory intelligence tool designed for use within our Industry.
Dedicated to improving efficiency and compliance with vigilance processes.