HomeEventsThe TechMed Series: Research on Human Subjects: patients, volunteers, users and public (session 6 of 7)

The TechMed Series: Research on Human Subjects: patients, volunteers, users and public (session 6 of 7) Accelerating implementation of your health innovation

SESSION 6 (OF 7): Research on Human Subjects: patients, volunteers, users and public

Clinical evidence on the safety and effectiveness of health innovations is key in their implementation. It is important to assess whether the risks of use are in reasonable proportion to the expected benefits. This asks for a qualitative and quantitative evaluation of the clinical benefit against the clinical risks, including undesirable side effects, in the target group and indication. Evidence can come from various sources however often human subject research has to be performed. The Scientific Research involving Human Subject Act (in Dutch: WMO) is applicable to this type of research. This workshop will give an introduction to this legislation and corresponding procedures.

General information

Where & When

  • 08 July 2021
  • 3-5 PM (Q&A after 5 PM)
  • Language: English
  • Online (after registration you'll receive the link to the livestream)

Course leader

Cindy Lammertink
Clinical research coordinator / lecturer  - TechMed Centre 

The purpose of the Workshop Series

This practical workshop series is available for everyone within Twente University that is involved in health technologies. These workshops are relevant for everyone in medical technology, eHealth, in-vitro applications, public health, wellbeing, home care or lifestyle.

This series is practical in nature and tailored to the needs within the University. During the workshops you will learn about regulations, documentation, how to successfully implement your innovation, research on human subjects, research data management and privacy. The workshop are hands-on with easy to use templates so you have everything you need to get started. This documentation is tremendously important if you intend to test your innovation on humans, license it or start a company. The earlier you start building it, the easier it becomes.

All sessions

03 June

Is my innovation a medical device?

Read more

10 June

Why risk management is important and how to implement it

Read more

17 June

What is design documentation and now to implement it

Read more

24 June

Why validation and verification are essential and how to implement them

Read more

01 July

Increase the chance of making and implementing a 'successful' product

Read more

08 July

Research on Human Subjects: patients, volunteers, users and public

Read more

Postponed

Research data management and Privacy

Read more

Organisation

This session is organized by the research program Sustainable Healthcare Technology (SHT), within the TechMed Centre institute. The mission of SHT is to improve the performance, uptake and impact of health technologies developed at the University of Twente that will contribute to making our healthcare future-proof. 

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