Medical-Device

Implementing ISO 13485:2016

This course will introduce the requirements of ISO 13485 and outline the steps for building an ISO 13485 compliant quality management system.

$549 USD

Introduction to ISO 13485 & FDA QSR

This course is for professionals in the medical device industry who want to learn about ISO 13485. Gain experience and a deeper understanding of the ISO 13485 Standard and... requirements.

$295 USD

European Medical Devices Regulation (EU MDR) Training

The European Medical Devices Regulation (EU MDR) applies to all manufacturers of medical devices sold in Europe. Gain an understanding of the EU MDR and how the new... requirements will affect your organization.

$899 USD

Introduction to 21 CFR 11

Learn about Part 11 of Title 21 of the Code of Federal Regulations, which establishes the United States Food and Drug Administration (FDA) regulations for electronic... records and electronic signatures.

$299 USD