Tracking announcements from health authorities is a time-consuming and error-prone process for pharmacovigilance teams. The Pleksus Regulatory Authority Website Monitoring Platform fully automates this process, ensuring that critical developments are noticed in time.
The platform monitors the websites — and the many pages beneath them — of the FDA, EMA, the World Health Organization (WHO) and the Turkish Ministry of Health, as well as the health authorities of many countries including France, the Netherlands, Canada, Italy and Australia, on an hourly basis, and reports newly published content in real time. All announcements are stored in a database and categorized by drug / active substance / medical device or any keyword. With this extensive history it is possible to access, re-screen and report on past screening results.
The main content monitored by the platform includes:
- Safety alerts
- Drug recall announcements
- Regulatory authority statements
- Guideline updates
- Marketing authorization and product information changes
- Other significant regulatory developments affecting medicines
Thanks to the automated monitoring infrastructure, teams no longer need to track authority websites manually, and the risk of missing critical announcements is significantly reduced.
The application is offered on a SaaS model and priced per registered drug, independent of the number of users.