Our Clinical Evaluation services

Our Clinical Evaluation services

Preview unavailable

You must log in or sign up to view this lesson.

LoginSign up

Understanding the EU MDR

Buy nowLearn more

1. Introduction

  • Introduction to the MDR
  • Supporting Information - Understanding the EU MDR
  • Structure of the MDR
  • MDR requirements
  • What is a medical device

2. Understanding requirements

  • Classifying medical devices
  • Making devices available on the market
  • General Safety and Performance Requirements (GSPRs)

3. QMS, PMS & Risk Management

  • Quality Management Systems & Post-Market Surveillance
  • Basic principles of Risk Management
  • Benefits of Risk Management

4. Clinical Evaluation

  • Clinical Evaluation & CERs
  • Basic principles of planning a CER
  • 5 common pitfalls for a CER
  • Our Clinical Evaluation services

5. Gap Analysis & Document Management

  • Gap Analysis Tool
  • Document Management
  • Importance of Document Management