Guided Pathways

Guided Pathways is a concept we have adopted from the educational sector. This approach is designed to “help each person to explore, choose, plan, and complete programs aligned with their career and education goals efficiently and affordably.”

Our research identified that many individuals working in MedTech have little to no prior experience in regulated industries. While technically competent in a vertical niche (say, Electrical Engineering), many individuals lack the horizontal skills needed to perform their jobs both quickly and efficiently.

We have created a Guided Pathway for each functional area in a MedTech company. Our approach:

* Clarifies paths to student education and business goals

* Helps students get on a specific path;

* Keeps students on path; and

* Ensures students are learning and applying those learnings.

These are the elements of the Guided Path for the;

Post Marketing Pathway

Monitor Device Performance and Ensure Long-Term Compliance

Getting FDA approval is just the beginning, you need to track device performance, safety, and market trends to maintain compliance and improve future designs. MedTech Tracker provides the data to help you track adverse events, manage risk, and refine your post-market strategy.

Airport Taxi/Approach way concept

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 Your Challenges

Tracking Device Safety Issues: Monitoring adverse event reports and product recalls.


Understanding Long-Term Performance Trends: Identifying device failures and patient outcomes.


Ensuring Compliance with Post-Market Surveillance (PMS) Requirement:  Meeting FDA & EU MDR post-market obligations.

 How MedTech Tracker Helps

Adverse Event Monitoring: Track FDA Medical Device Reports (MDRs).


Post-Market Surveillance Data: Analyze device safety trends over time.


Competitor Performance Insight: Compare market trends and product lifecycle trends.

Stay Ahead in Post-Marketing Compliance

MedTech Reference Guide

Adverse Event Monitoring

We can help you monitor the adverse events for your product codes by providing FDA open data, MAUDE reports, and post-market surveillance insights. Identify potential safety issues early and make informed decisions to maintain compliance and protect patients.

Post-Market Surveillance Data:

We can help you analyze device safety trends over time with comprehensive post-market surveillance data. Track FDA open data, recall patterns, and practical performance insights to ensure compliance and continuous product improvement.

Compliance with Post-Market Surveillance (PMS)

Our data solution help you efficiently track and analyze adverse event data, ensuring regulatory compliance and enhancing product safety.

Documents

Over 200,000+ PDFs available. Still Can’t Find What You’re Looking For?

MedTech Reference Guide

MedTech Reference Guide

Gain a better understanding of your product code, access essential medicare data and reimbursement codes. Download the MedTech Reference Guide today and request your free Regulatory and Reimbursement Report to stay ahead in the industry.