Vigilance Monitoring on AutoPilot

Consistent and comprehensive reporting of Adverse Events and Recall data for your entire device portfolio

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.

Illustration of an online dashboard displaying data analytics and reporting features for medical device vigilance monitoring and adverse event tracking.

Global Data Sources

Our team and system can collect your Adverse Event data from any desired databases.

Illustration of stacked files and a document titled "Historical Reports," representing data organization and accessibility for vigilance monitoring in medical devices.

Vigilance Reports on Any Interval

Our team can search and review on timeframes as short as Weekly, or as long as Yearly.

Online dashboard interface for medical device vigilance monitoring, displaying data flow and report management.

Online Dashboard

View all data, finalized vigilance reports, and trending analysis online.

What Clients Say About CiteMed’s Vigilance Monitoring & Reporting

Forbes logo, representing a trusted source in healthcare innovation and compliance.
Yahoo Finance logo, representing financial insights and news relevant to healthcare compliance and innovation.
CiteMed logo representing regulatory consulting services for medical device compliance with EU MDR regulations.
NBC logo, representing a trusted media outlet, featured in a section promoting CiteMed's regulatory consulting services for healthcare compliance.
Fox News Channel logo, representing media coverage relevant to healthcare compliance and innovation discussions.
CNBC logo representing business news and financial insights, relevant for compliance and regulatory discussions in healthcare.

Our Clients Say

Worry-Free EU MDR Compliance

Magnifying glass over documents representing search and analysis for Clinical Evaluation Reports (CER) and regulatory compliance in medical device submissions.

1. Searching and Data Ingress

CiteMed (Through Automation and Careful Human Auditing) Collects Adverse Event Data from all of your chosen global sources

Illustration of two document templates with images and text sections, representing regulatory affairs and EU MDR compliance for medical devices.

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).

Illustration of a secure digital interface with data charts and documents, emphasizing regulatory compliance and data management for medical device manufacturers.

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.

Cloud symbol with medical cross, and documents labeled CER and PMS, representing regulatory templates for Clinical Evaluation Reports and Post-Market Surveillance in medical device compliance.

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

Computer monitor displaying adverse event data and reports, illustrating CiteMed's dashboard for medical device regulatory compliance and vigilance reporting.

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.

GET A QUOTE
BSI Group logo, symbolizing regulatory compliance expertise for medical devices in the context of EU MDR evaluations.
SGS logo representing quality assurance and regulatory compliance in medical device evaluation and clinical documentation.
TÜV SÜD logo, symbolizing quality assurance and compliance in medical device regulations, relevant to CiteMed's consulting services for EU MDR submissions.
TÜV Rheinland logo, symbolizing quality assurance and compliance for EU Medical Device Regulation (MDR) processes.
NSAI logo, representing quality assurance and regulatory compliance in medical device evaluation and submissions.

What’s Included in Your Vigilance Reports?

Dashboard interface displaying adverse event reports and trending data for medical device vigilance monitoring.

Trending Data

Trending Data (based on search results, and your previous reports)

Dashboard interface displaying adverse event report summaries, trending data, and search results for medical device vigilance monitoring.

Result Counts

Summary Table and Count of All Results by Data Source

Illustration of two overlapping documents with alert icons, representing vigilance reporting and adverse event tracking for medical devices.

Expert Filtered Search Results

List of Relevant Adverse Events/Recalls Retrieved

Illustration of two documents representing vigilance reporting and adverse event monitoring for medical devices, featuring icons for security and global data access, aligned with CiteMed's centralized platform for AE Reports.

Full Search Archive

Full Appendix of All Search Results. Archived

Your Vigilance Reporting Plan Starts Today

GET A QUOTE

The Price of Delays

Blue clock icon representing expedited timelines in regulatory consulting services for EU MDR compliance.

Regulatory Staff’s Time

Let your CER writer’s focus on the draft while we deliver the clinical literature search.

Blue thumbs-up icon representing quality service and client satisfaction in regulatory consulting for EU MDR compliance.

Loss of market share to competition

Don’t lose precious ground to competitors already operating the EU markets.

Blue diamond icon representing quality and value in regulatory consulting services for medical devices.

Time to market

Lost Revenue
Even the smallest oversights can lead to endless correspondence with your Notified Body (who is flooded with work and will be even slower to respond)