This course is designed to provide participants with an understanding of ISO 14971:2007 – Risk Management for Medical Devices, and the impact that the FDA’s CFR 820 has on their decision-making process at medical device manufacturing firms. This one-day training course helps medical device professionals gain an understanding of how CFR 820 will affect their processes and procedures to ensure compliance to the US FDA. Participants will also understand how CFR 820 applies to ISO 13485:2003.
Public Course Dates
On-site group training is delivered at your place of business and can be customized to meet your specific requirements. Contact The Business Resource Centre to schedule your next on-site group training event.
Please call 1-888-535-1401 or fill out the form below to request a quote.
Public training is available for this course. Locations and dates can be found using the form below. Please fill out and submit the form to register for this course.
Online training is available for this course. Please fill out and submit the form to register for this course.