Post-Market Surveillance of Medical Devices

Search, analyze, and export relevant events from FDA Recalls, MAUDE, BfArM, MHRA, Pubmed, Europe PMC, ClinicaTrials.gov, NVD cybersecurity vulnerabilities, and more data sources. All Recall, Adverse Events, Cybersecurity, and Scientific Literature databases you need in one place.

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Extensive Data Insights & Analysis

Access a unified platform connecting top data sources like FDA Recalls, MAUDE, BfArM, MHRA, PubMed, Europe PMC, ClinicalTrials.gov, and NVD—all in one place. Need more? Contact us to add additional databases.

Find the most comprehensive insights on medical device events, research articles, and cybersecurity vulnerabilities to enhance product development and post-market surveillance.

Go beyond public BfArM and MHRA databases with advanced OCR, extracting data from scanned PDFs to uncover hidden, non-searchable information. Don’t miss critical insights.

Unified platform for accessing FDA Recalls, MAUDE, BfArM, MHRA, PubMed, ClinicalTrials.gov, and more databases. Streamlined post-market surveillance with advanced search, data extraction from PDFs, and comprehensive insights on medical device safety and cybersecurity.

Unlock deeper insights and streamline your post-market surveillance with our robust advanced search capabilities.

Easily define specific search parameters across companies, products, FDA product codes, keywords, device problems, and more.

Break through 10x the FDA's 500-record limit to access comprehensive data and uncover critical insights.

Our intuitive search tool empowers you to quickly locate relevant safety events, potential vulnerabilities, and supporting scientific literature.

Advanced search tool for post-market surveillance, enabling precise queries across FDA product codes, keywords, and device issues. Access 10x beyond the FDA's record limit to uncover critical insights and streamline medical device safety analysis.

Unlock powerful insights with robust analytics, interactive trend charts, and comparison tools to quickly analyze and uncover key events.
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Our intuitive filtering options let you sift through thousands of records using product name, manufacturer name, keywords, or even custom tags.

Leverage advanced filter capabilities for precise queries to locate specific events or explore broader topics to streamline your data analysis.

Identify Use Errors instantly with our AI-powered detection tools, ensuring proactive risk management.
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Stay ahead with smart Alerts and Notifications—get daily updates on new adverse events, recalls, scientific publications, or cybersecurity vulnerabilities that align with your saved searches.

Analytics dashboard with interactive trend charts, advanced filtering, and AI-powered tools for detecting use errors. Quickly analyze medical device events, set custom alerts for recalls, publications, and vulnerabilities, and receive real-time notifications to enhance proactive risk management.

Easily export comprehensive data for customized reporting, offline analysis, or seamless integration with your quality management systems. Download presentation-ready charts.

Ensure compliance with our comprehensive audit trail, automatically tracking every entry and decision for full transparency and reproducibility in your post-market reviews.

Achieve superior data integrity for regulatory submissions.

Comprehensive data export and audit trail features for customized reporting and quality management. Download presentation-ready charts, track every entry for transparency, and ensure compliance in post-market reviews and regulatory submissions.

KNOWN USE ERROR

AI-Powered Screening

Identify Use Errors instantly with AI-powered detection tools. Our system automatically highlights possible Use Errors, pinpoints specific use error keywords in the event data, and provides clear explanations of the use error to help you understand and address risks proactively.

Critical User Actions

Uncover root causes with AI-powered analysis of Use Errors. Our algorithm identifies user actions leading to errors, the resulting failures, and generates a correlation map. Quickly gain deep insights into the most common actions and failures to drive informed improvements.

Import Internal Complaint Data

Enhance your analysis by importing internal customer complaint data into our platform. Easily import, format, and validate your data, then leverage our AI-powered Use Error analysis tools to detect use errors, user actions, failures, and correlations—unlocking actionable insights for proactive risk management.

The Best Solution for Post-Market Surveillance of Medical Devices

Centralized Post-Market Surveillance Analysis

Access all relevant data—from complaints to literature reviews—in one powerful platform, streamlining your workflow and saving you valuable time.

Customizable Data Searches

Define precise search criteria across companies, product categories, and keywords. Save searches, analyze results, monitor trends, and find relevant events.

Real-Time Updates for Proactive Risk Mitigation

Track product performance with real-time updates and alerts, enabling you to proactively identify and address potential safety issues and maintain regulatory compliance.

Actionable Insights with Advanced Analytics

Make informed decisions with robust analytics, interactive trend charts, and comparison tools, empowering you to proactively improve product quality and patient safety.

Flexible Data Export for Deeper Analysis

Export comprehensive data sets in multiple formats for customized reporting, offline analysis, and seamless integration with your existing quality management systems.

Enhanced Product Quality & Patient Safety

Proactively identify and resolve product quality issues, leading to improved device reliability, enhanced patient safety, and demonstrable regulatory compliance.

Post-market surveillance is a required activity for medical device manufacturers per FDA's 21 CFR and EU’s Medical Device Regulation (MDR). PostMarketMonitor will eliminate:

Medical Device Insights

Expert Insights & Resources for Medical Device Safety

Post-Market Surveillance

Late Reporting of Medical Device Deaths and Injuries to the FDA: A Major Gap in Postmarket Surveillance

Nearly a third of medical device adverse event reports from manufacturers to the FDA were submitted late, often more than six months after the manufacturer was notified

Ways the Trump Administration is Transforming the MedTech Industry

A balanced analysis of five key ways the Trump administration is reshaping the MedTech industry—including FDA regulations, AI advancements, tariffs, leadership changes at HHS, and impacts on post-market surveillance—highlighting both the opportunities and challenges for innovation and patient safety.

48 Minutes to Disaster: How Phishing Attacks Exploit Weaknesses

A recent manufacturing sector breach demonstrates how attackers combine phishing tactics with legitimate tools to quickly gain control and move laterally within a network, emphasizing the need for enhanced detection and prevention strategies.

Try the Professional Plan Free for 2 Weeks!

Explore all features of PMM for 2 weeks to see how it can simplify your post-market surveillance. If you cancel before the trial ends, your credit card will not be charged

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