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TechMed workshop series (6/6) - Controlling the process Medical devices: Controlled from design to production

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The workshop & Course aim

Medical devices: Controlling the process from design to production.

In order to market medical products, many requirements must be met. Within the European Union, these requirements are imposed by Medical Device Regulation (MDR), formerly known as Medical Device Directive (MDD). For one thing, the development of medical devices is subject to strict conditions. Furthermore, the entire production process must be validated in full. And in addition, setting up a supply chain is a key element of the production system, in which continuity and quality are paramount.

All logistical aspects with regard to the purchasing and verification of materials, as well as (worldwide) shipping of complete end products play an important role. Other business aspects are equally important. This is certainly true for medical products, where each country has its own rules and regulations to market products, both in Europe and beyond.

detailed overview

16.00 – 16.15

Registration & Coffee

16.15 – 16.45

Introduction to medical market

16.45 – 17.15

Medical Device Regulations and standards for CE

17.15 – 17.45

Development of medical devices

17.45 – 18.15

Design transfer activities

18.15 – 18.45

Food

18.45 – 19.15

Production and service of medical devices

19.15 – 19.45

Business aspects

19.45 – 20.00

Questions, networking and drinks

FOR WHOM

This workshop is relevant for everyone who is working on a medical device (prototype/product), such as engineers, project managers and quality managers.

WHERE & WHEN 

  • 18 April 2019
  • 16:00-20:00
  • Carré 3.022, Auditorium ECTM
  • University of Twente, Drienerlolaan 5, Enschede

SPEAKER 

Unitron Group BV
Mario Steel

Unitron develops and manufactures complete products, such as medical equipment and specific industrial products. This may involve the realisation of a completely new concept, but also the modification and optimisation of existing products.

This, in combination with our experience and business strenth, will result in a complete business concept. Unitron is active in several markets throughout the world. 

REGISTRATION

We welcome a maximum number of 50 participants. Participation is free of charge. We will count on your participation for creating working groups and catering. If you cannot attend the event for which you have already registered, we kindly ask that you let us know. Simply e-mail techmed-events@utwente.nl.

ORGANIZATION: TECHMED WORKSHOP SERIES 

This workshop is part of the TechMed Workshop Series ‘Remove the Barriers to Market Readiness’. This one-year-course of workshops covers the most important, but also most challenging, topics required for the development and production of a safe, reliable and useful medical device. The workshops are organized for (future) entrepreneurs in the medical device industry, take place every 2 months on an afternoon and focus on one specific topic every session. It is possible to attend the complete course, but also separate workshops.

The TechMed Workhsop Series is part of the TechMed Proeftuin. By sharing their knowledge and expertise in the workshops series the TechMed Proeftuin partners aim to bring medical innovations 1 TRL level further and closer to a successful market introduction. The TechMed Proeftuin receives funding from the European Regional Development Fund (ERDF) of the European Union; the Workshop Series can therefore be offered free of charge.