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.
Global Data Sources
Our team and system can collect your Adverse Event data from any desired databases.
Vigilance Reports on Any Interval
Our team can search and review on timeframes as short as Weekly, or as long as Yearly.
View all data, finalized vigilance reports, and trending analysis online.
Our Clients Say
I’ve never seen such a streamlined process for literature search and review. CiteMed produced elegant reports that were easy to read despite their length and incredible detail
Quality Director, Medline Industries
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.
Take Us For a Test Ride
Get in touch today to see a demo, sample vigilance report and our pricing.