Your Vigilance Data in One Place
It’s a full time job searching and compiling Adverse Event Data for all of your medical devices each month, quarter,
and year. With the Cite Medical Vigilance Module, all of your data (reviewed by the team) is accessible in one single location.
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Worry-Free EU MDR Compliance
1. Searching and Data Ingress
CiteMed (Through Automation and Careful Human Auditing) Collects Adverse Event Data from all of your chosen global sources
2. Expert Review of All Search Results
Our team of medical writers reviews the results and classifies any relevant Events for you to be included in the next Vigilance Report. (this is optional).
3. All Results Made Visible on Your Dashboard
Search results as well as our team’s reviews/classifications are immediately available for you to access on your CiteMed Dashboard.
4. Vigilance Report Document Is Delivered
On your chosen time interval, CIteMed delivers an Adverse Event Report to you via email and accessible directly on your CiteMed Dashboard.
All Your Vigilance Data In One Place
If You Are:
Short on staff and resources to conduct multiple Vigilance reports every quarter.
Perfectionists that want a consistent system and operating procedure to satisfy Post Market Surveillance requirements.
In need of a single centralized platform to securly store your AE Reports and trending data over time.
What’s Included in Your Vigilance Reports?
Trending Data
Trending Data (based on search results, and your previous reports)
Result Counts
Summary Table and Count of All Results by Data Source
Expert Filtered Search Results
List of Relevant Adverse Events/Recalls Retrieved
Full Search Archive
Full Appendix of All Search Results. Archived
