The physical embodiment of a medical technology and its interaction with the healthcare professional or patient
end-user can make or break its adoption by the wider market. At the same time med-tech product design is carried out in a highly regulated sector where demonstration of compliance to international standards is critical to achieving market authorisation. This event in partnership with the Medical Technologies Innovation Facility (MTIF) brings together speakers from the NHS, industry and academia to provide considered insights into the area of Med Tech product design.
The webinar will address:
-Balancing safety, function and form – how using professional design services can save project time and costs
-The role of human factors in assessing med-tech product design
-The value of obtaining end user acceptance data though expert clinical evaluation
-Design and Achieving Regulatory compliance
This webinar is open to all organisations seeking insight into medical product design and the particulars of clinical evaluation and human factors assessment.
There will also be an opportunity to pose your questions to our presenters in a Q&A session after the presentations.
This free to attend event is held as part of the INSTILS programme – a project part-funded by the European Regional Development Fund, click here to be re-directed to further information about the project. This event is classed as State Aid to participating businesses, the value of which is £190, but is delivered completely free of charge to participants.
Please note: whilst this event is held as part of the INSTILS programme, this event is not restricted to those in the D2N2 area.