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Learn about the medical device industry and how to bring new products to market 510K, PMA, De Novo, ISO13485 and beyond!

What you will learn

Learn how medical devices go from idea to product

Understand the 510K and PMA submission process for medical devices

FDA regulatory pathways including 510K, PMA, De Novo, IDE, HDE

Risk management and quality in device development

Learn how to research new devices and companies

Understand medical device career paths and opportunities

Description

The medical device industry is growing rapidly, providing great opportunities for innovators, experts and entrepreneurs. This course will provide a detailed overview of the way in which new devices go from concept to product, providing you with a starting point to develop a deep understanding of this complex and fast-moving business space.

We will cover all of the key components of bringing a new device to market, including:


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  • Paths to Market, including the 510K, PMA, HDE and other commonly used pathways
  • Clinical trials of medical devices, including IDE, submissions, records and reporting
  • Risk management and quality in device development

During this course we will also cover the publicly available information sources that will enable you to research device companies and understand their value. We will cover medical device databases that allow you to research marketed medical devices. We will cover clinical trial databases that allow you to research planned and ongoing trials of medical devices. Links to these freely available resources will be provided.

This course will be a valuable resource for anyone interested in developing their basic knowledge of the medical device industry. For students and recent graduates in medical device engineering, this course will help you develop a knowledge of the industry and the regulatory steps that companies use to bring new innovations to market. For project managers, this course can help you to learn about this industry and equip you to manage medical device development projects. For professionals working in related fields, this course will provide an overview of the medical device industry.

English
language

Content

Introduction

Introduction
Medical Device Industry
Researching Medical Device Companies
Medical Device Careers

Regulation of Medical Devices

MD100 Medical Devices Overview
MD110 Medical Devices Definitions
MD115 Medical Device Regulations
MD120 Medical Device Regulations History
MD130 FDA History
FDA Regulations

Path to Market

MD200 Path to Market
MD210 Device Classification
MD230 510K and PMA
MD232 Predicates
MD234 FDA Databases

Clinical Trials

MD300 Clinical Trials
MD310 Investigational Device Exemptions (IDEs)
MD330 IDE Submissions
MD340 IDE Records & Reporting
MD350 Researching Clinical Trials

Quality Systems

MD400 Quality Systems
MD405 Risk Management
MD410 GXP
MD412 GLP
MD414 GCP
MD416 GMP
MD418 Supply Chain
MD420 Design Controls
MD430 Design Inputs
MD440 Design Outputs
MD450 Verification and Validation
MD460 Design Transfer
MD470 Design Changes
MD480 Documentation

Medical Device Submissions

MD500 Medical Device Submissions
MD510 FDA Interactions
MD520 510K Submissions
MD530 510K Content
MD540 510K Abbreviated
MD550 510K Special
MD580 PMA Submissions
MD590 Change Communication

Post-Market Surveillance

MD600 Post Market Surveillance
MD610 MDR
MD620 Recalls
MD630 522 Postmarket