TechMed Series

BADGE INFORMATION

First name *

Last name *

Organisation *

My organisation is a *

Occupation/position *

PART 2: YOUR OWN CASE

Description of the development of your Medical device: *

PART 3: MATCHMAKING TOOL

A (digital) face book will be created for the event. This face book contains the information from parts 1 and 3. In order to give a good impression of yourself and what you are looking for, we advise you to complete the questions below (although not required to complete the registration). This information is only accessible to the TechMed Series partners (Holland Innovative, Panton and Unitron) and will be presented (on a screen) during the 8 TechMed Series.

These keywords describe my work (max 5):

My distinctive work related qualities are:

I want to get in contact with / I'm looking for:

My profile picture:

I allow my email address to be published in the face book.

I already filled in these question (because I have participated in other sessions of The TechMed Series).

PART 4: EVENT & COMMUNICATION

I want to pitch my organisation/problem/product/question during the part "Learn from the best".

Special diet requests (such as allergies) or other wishes:

Comments:

Email address *

I agree that my contact details may be used by the University of Twente for mailings about future TechMed events and activities.

Yes

I already signed up for the newsletter of TechMed Centre

I agree that, accordance with the GDPR/AVG regulation, photos made during the event can be publicated.

Yes

Click here to read the privacy statement

By checking this box, you acknowledge that you have read and understood the privacy statement of the University of Twente *

PARTICIPATE 1 OR MORE SESSION(S)

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.

Below you can choose one or more sessions of this whole Series. During every session one phase/process will be explained by healthcare professionals.

Click on every session for more information.

I will visit:

Session 1: Getting started with the CE marking - 29 October 2019

Session 2: Involving end users in the design process - 26 November 2019

Session 3: Risk management in medical devices - 10 December 2019

Session 4: Software as a medical device - 23 January 2020

Session 5: Clinical evaluation of your medical application - February 2020

Session 6: Prototyping and production of medical devices - March 2020

Session 7: Design verification & validation - April 2020

Session 8: Finding funding for your R&D - May 2020