Learn regulatory approaches for medical devices

WATERLOO, Ont. – Are you an innovator seeking to market your product in the Canadian healthcare sector? Or a hospital manager, engineer or scientist looking to test new equipment? It is up to the quality and regulatory representatives of an organization to understand and apply the regulations and standards to their products.

There are some key ways of approaching this area of quality and regulatory in medical devices with a pragmatic mindset and flexible way of thinking that can save time and effort.

Pragmatic Quality & Regulatory Approaches for Medical Devices
8 Sessions, 8 Hours
Live. Interactive. Online via Webex.
Weekly, April 21 – June 16, 2023 | 12:00 – 1:00 PM ET
No Session May 5, 2023

Competencies Achieved Upon Completion of the Course
Participants will be able to:

• Identify a Regulatory Strategy for an existing or new product.
• Create an outline of a Quality Management System for Hardware and/or Software Products.
• Apply best practices on a pragmatic approach to Regulations and Standards.

Your instructor:
Christie Eby (pictured), Director, Process Excellence, Quality Regulatory, Intellijoint Surgical; Instructor, NIHI

Christie Eby brings over 20 years of experience in the health IT field, in the areas of: Medical Device Regulatory, Quality Systems, Change Management, Process Improvement, Facilitation, Software Development and HR. Christie has recently joined Intellijoint Surgical as Director, Process Excellence, Quality Regulatory. For the previous 10 years she was part of the management team at Client Outlook Inc., purchased by Mach7 Technologies in July 2020.

Registration and more information.