Design verification & validation
THE WORKSHOP
Verification and validation are two essential steps in the development process of a medical device. When applying for CE certification of your medical device, you have to be able to apply and show verification and validation. By means of verification and validation you show that your product and production process meet the requirements and are suitable for the intended use. This workshop will cover the basics of validation and verification, how to set op experiments to actually validate and/or verification your medical device. We share multiple clinical experience examples during the workshop.
FOR WHOM
This knowledge is essential for everybody involved in or responsible for medical device development, both from a technology perspective as from a management perspective. Also it is relevant for everyone who is working on a medical device (prototype/product), such as engineers, researchers, projectleaders.
WHERE & WHEN
- 7 May 2020
- 15.00 - 17.00 (Online doors open from 14.45, Q&A after 17.00)
- Entrance: free
- Language: English
- Location: Online. After registration you will get a link to the meeting.
TECHMED SERIES
THE PURPOSE OF THE TECHMED SERIES
The goal of the TechMed Workshop Series ‘Remove the Barriers to Market Readiness’ is to offer and share knowledge and expertise. The substantive sessions are organized for researchers and (future) entrepreneurs in the medical device industry take place every month. It is the aim of the TechMed Series to bring medical innovations a TRL level further and closer to a successful market introduction. The fee for the workshop series must cover the costs, and are not for profit.
The TechMed Series "Remove the barriers to market readiness" is a one-year-course of workshops for (future) entrepreneurs and scientists in medical technology. The series covers the most important, but also most challenging topics required for the development and production of a safe, reliable and useful medical devices. Following the successes of the past years, we have updated the program to fit your needs on the road to market readiness. During the course of 1 year, 8 sessions are organized, taking place every month on an afternoon and focusing on one specific topic every session. During the sessions, you will work in groups to bring new knowledge to the test. There are no obligations, but we highly encourage you to bring your own case into the discussion! It is possible to attend the complete course, but also separate sessions.
8 INSPIRING SESSIONS
1 of 8 | Getting started with your CE mark. | |
2 of 8 | Involving end users in design process. | |
3 of 8 | Risk management. | |
4 of 8 | Software as a medical device. | |
5 of 8 | Clinical evaluation of your medical application. | |
6 of 8 | Prototyping and production of medical devices. | |
7 of 8 | Design verification & validation. | |
8 of 8 | Finding funding for your R&D. |
ORGANIZATION & PARTNERS
This session is part of the TechMed Workshop Series ‘Remove the Barriers to Market Readiness’. The events are organized for (future) entrepreneurs in the medical device industry, take place every month on an afternoon and focus on one specific topic every session. By sharing their knowledge and expertise in the TechMed Series the partners aim to bring medical innovations 1 TRL level further and closer to a successful market introduction.
The TechMed Series is a spin-off from the TechMed Proeftuin, an initiative by Holland Innovative, Unitron, Panton and the University of Twente.
THIS EVENT IS POWERED BY:
