Back to previous page

Medical Devices: EU Regulations

Price

$535*

Location

At your desk

Completion Time

5 Hours

Reference No: T1708009-RAP

Apply for this event
Event Description

This course provides a solid understanding of medical device regulation in the EU. It covers the history of medical device regulation in Europe and follows the regulatory requirements throughout the product lifecycle. You will gain a strong foundation of the key elements of the EU directives governing medical devices. These include: Active Implantable Medical Devices Directive (AIMDD) 90/385/EEC, Medical Devices Directive (MDD) 93/42/EEC and In Vitro Diagnostic Devices Directive (IVDD) 98/79/EC in their latest revision, including the 2007/47/EC amendments to AIMDD and MDD. This course examines how devices are classified, and the effect classification has on labeling, registration, marketing and postmarketing requirements. 

At A Glance

  • Target Audience: This program is designed for new regulatory professionals and others in related departments interested in understanding the basics of EU regulation of medical devices.
  • Learning Level: Basic
  • Total Length of Course: 5 Hours
  • RAC Points: 5
  • Formats: Web and Tablet

Learning Objectives

Upon completion of this course, participants should be able to:

  • Explain and differentiate between the scope of the three EU device directives
  • Outline how medical devices are classified using the European regulatory framework
  • Identify the important contents of each EU directive
  • Discuss the general requirements of preclinical and clinical testing in Europe
  • Describe the conformity assessment pathways for obtaining CE marking
  • Cite the key requirements for postmarketing surveillance
  • Explain the overall regulatory requirements for medical devices in the EU

Lesson Titles

  • Lesson 1: History of Medical Devices in EU
  • Lesson 2: The Medical Device Directive (MDD)
  • Lesson 3: The IVDD, AIMDD plus Other Directives and Guidance Documents
  • Lesson 4: Standards, Quality Assurance and Risk Management
  • Lesson 5: Postmarketing Requirements

*Cost

RAPS Member: $535.00
Non RAPS Member: $735.00

Other terms and conditions apply when applying for this course.

See What Others Are Saying About This Conference On Our Forum

Forum Link - Medical Devices: EU Regulations

Applicant Requirements
  • New regulatory professionals
  • Others in related departments interested in understanding the basics of EU regulation of medical devices
Reference No: T1708009-RAP
The Regulatory Affairs Professionals Society (RAPS) is the largest global organization of and for those involved with the regulation of healthcare and related products, including medical devices, pharmaceuticals, biologics and nutritional products.

Come and join our community!

We are ready and waiting for you

This site uses cookies. By continuing to browse the site, you are agreeing to our use of cookies.

Read more or Hide this message