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;

Technical Pathway

Design and Develop MedTech Devices with Regulatory-Backed Data

Technical leads, R&D engineers, and product developers need structured data to ensure safety, compliance, and performance. MedTech Tracker provides real-world regulatory and testing insights to help you make informed design decisions.

This is MedTech Tracker Technical pathway concept using the hanger airport

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 Your Challenges

  •  Navigating Regulatory Complexity: Finding correct product codes, performance benchmarks, and testing criteria.

  •  Avoiding Device Failures: Learning from past adverse events and competitor recalls.

  •  Ensuring Manufacturing Compliance: Accessing FDA safety and testing standards.

 How MedTech Tracker Helps

  • Regulatory Roadmap for Engineers: Identify pre-market approval steps and compliance requirements.

  • Medical Device Reporting (MDR) Database: Access historical failure reports to improve safety.

  • Manufacturing and Performance Insights: Get data on testing, electrical safety, and device compliance.

Take the next step

MedTech Reference Guide

Technical Roadmap for Engineers

We offer a Device Technical Roadmap for Engineers. We can guide you through design specifications, testing requirements, and regulatory standards. Streamline your development and ensure device compliance from prototype to market.

Medical Device Reporting (MDR) Database:

We provide access to the Medical Device Reporting (MDR) Database, helping you track and analyze adverse events for regulatory compliance. Our expert guidance ensures seamless reporting, minimizing risks and enhancing patient safety.

Device Manufacturing and Performance Insights:

Gain valuable Device Manufacturing and Performance Insights to ensure compliance, optimize production, and enhance product reliability. Our expertise helps you analyze performance data, identify risks, and maintain regulatory standards with confidence.

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.