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An Introduction to the Regulation of Medical Devices
Course Summary
This module provides an introduction to the basics of medical device regulation, especially the requirements that manufacturers must meet in order to market devices in Europe and the USA.
We explain what medical devices are and give examples of the various types. We outline the principles of their regulation and the criteria for placing them on the market. We identify major players in regulation worldwide.
We then outline prominent characteristics of the regulation of medical devices in the USA and in Europe. The module is up to date with the current upheaval in European Union legislation on medical devices.
Purchasing Information
When you have completed your course order, Zenosis will finalise the setup of your course materials and contact you on the email address that you provide in your order. You can expect this process to be completed within one business day (using the UK business calendar) of completing your payment.
It is therefore essential that you use your real email address for your order, or indicate in the purchase notes the email address to be used for the course set-up, and check that any messages from Zenosis or grapl are not lost in your junk or spam folder.
You will have access to the course module(s) for a period of 180 days after your purchase is complete.
Detailed Course Information
Learning Objectives
• Define and give examples of the various categories of medical device
• Outline the principles of medical device regulation and the criteria for placing devices on the market
• Identify major players in the regulation of medical devices worldwide
• Identify legal statutes and sources of regulatory guidance on medical devices in the European Union and the USA
• Outline prominent characteristics of the regulation of medical devices in the USA
• Outline prominent characteristics of the regulation of medical devices in the European Economic Area
Who will benefit from this course
This module provides essential training for all personnel concerned with the development, regulatory compliance, or marketing of medical devices.
It is especially suitable for induction training of entry-level staff.
Module Outline
• Module overview
– An outline of the module’s scope and objectives, and notes on terminology.
• Medical devices and their regulation
– In this session we explain what medical devices are and how they differ from medicinal products.
– We define various special categories of such devices. We identify basic principles of their regulation, including risk classification.
– We outline requirements for technical documentation, clinical data, and post-market surveillance and vigilance.
– Finally, we identify the major players in regulation.
• Regulation of medical devices in the USA
– In this session we outline prominent characteristics of the regulation of medical devices in the USA.
• Regulation of medical devices in Europe
– In this session we outline prominent characteristics of the regulation of medical devices in the European Economic Area.
• Assessment
Roles
Research, Regulatory, Manager, Other
CPD Points
1
Region
Level
Introductory
Course Study Time
Approx 1 hour
USA, Europe