2653 S. Iris St.
Lakewood, CO
80227 USA

303-985-7942

21 CFR 820 Training On-line Executive Overview Benefits of 21 CFR 820 compliance Regulation content Implementation strategies 21 CFR 820 Implementation resources

21 CFR 820 On-line Executive Overview

This two-session, three-hour on-line training course is for executive management, department managers, engineers and other personnel of medical device manufacturers that plan to or started implementation of a Quality Management System compliant with the FDA 21 CFR 820 requirements.  This short course provides management with a sound understanding of the 21 CFR 820 requirements. You will learn the intent of the  regulation, its content, what organizations are subject to compliance and what it will take to implement it.  At the conclusion of the course there will be time for questions and answers to address your specific needs. 

This course is delivered via video-conference.  The participants are expected to have head sets for their computers and have access to the Internet.  Before the presentation, participants will receive an e-mail with a link to our video-conference.  When you login, you will see your instructor and will be ready for your presentation.

Cost:  $350 USD

Participants:  Maximum 5

Course materials:  A copy of the presentation in MS Power Point format

Included:  21 CFR 820 / ISO 13485 Correspondence matrix and ISO 13485 Quality Manual 

Call us today to schedule your training or discuss your specific ISO management system needs!