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Development team working infront of a large screen in a lab

Product development of biomedical devices

Tampere University



Course dates


Application period



1400,00 + VAT 24 % (Price incl. VAT 1 736 €)

Language of instruction


Study fields

Management, Administration and Economics
Technology and Natural Sciences
Health and Welfare
Data Processing and Information Technology

Organising unit

Tree – Continuing Education

Study level

Other studies

How to be able to apply funding, guarantee the patient safety according to regulatory requirements and still please the customer and make profitable business?

Product development of different health technology products or solutions could be thought as a multi-dimensional project. In this course, a product development project for a biomedical or health technology product is planned from idea to finished product. Instead of lectures, we work as R&D teams. The NABC model, teamwork and pitching will become familiar.

In addition to various plans such as project plan, biological and clinical evaluation plans, and go to market plan, a schedule and budget for the project are made and the cost structure of the product is determined. At the end of the course, the product and project are presented to a jury which evaluates them.

Target group

This course is targeted for those who are working or willing to work in health technology companies in different roles in R&D, quality and regulation, production, marketing and sales and management. The course gives essential knowledge also for health technology start-ups and anyone who wants to update his or her knowledge about product development and commercialization in health technology field.

You can also participate in the course with your company's own team and design product and project that suits your company's needs. The course can also be customized for a company or organization.

This course is part of Health technology solutions – product development and commercialization (programme). Get acquainted with the programme and other courses included in it.

The programme offers a formal additional education for a “Person responsible for regulatory compliance” required by the new EU regulations in Medical Devices Regulation (MDR) and In-vitro Diagnostics Regulation (IVDR).