Medical device companies have to overcome many challenges when bringing a new product to market. A key element is understanding the medical device regulations (MDR), which involves all stages of product development from design and manufacture, to quality and marketing. By complying with such regulations, manufacturers can be sure products meet the necessary certification and verification standards.
This four-day, online course is designed to support innovative companies who work in the design and manufacture of medical devices to gain a stronger understanding of the processes involved when developing new technologies in a healthcare setting.
This course has limited spaces available. Should you be unable to attend, please cancel your booking via Eventbrite to allow us to re-allocate your place.
Failure to cancel and or attend may result in you being removed from any future courses.
The course will provide an overview of the medical device regulatory affairs and how their integration fits with the management of healthcare technology and the processes involved in adopting the medical devices.
It is intended that this course will also provide companies and individuals with an understanding of how to liaise with the medical sector such that higher uptake of innovative medical devices can be achieved.
By taking part in this course, participants will:
The course is targeted at:
This course is being delivered in partnership with Heriot-Watt University and will feature lectures and presentations from the following experts:
Dates & Venues
|Date||15, 22, 29 June, and 7 July 2021|
|Duration||10.00 - 16.30|
In collaboration with