Sterilisation and biocompatibility are must do actions for new medical devices. Based on the materials and components used, complexity and configuration of the device, a potentially suitable sterilisation method has to be selected, its influence on the device evaluated and efficacy demonstrated through biological validation experiments. On the other hand, biological investigations, either in vitro or in vivo should confirm biological safety of the device in order to be allowed for further functional studies and clinical trials.
In this webinar, you will learn an approach for selecting the most suitable sterilisation method for optogenetic implants and the necessary biological tests needed to prove the device biocompatibility.
REGISTRATIONS FOR THIS WEBINAR ARE CLOSED
Date
30th January
Host
Dr. Biotza Gutiérrez
Optogenerapy project Coordinator, Eurecat
Presenter
Dr. Radoslaw Wach
Scientific and Lecturer, Lodz University of Technology
You should be interested if you are…
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An academic or researcher working with biomaterials
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A company, start-up or manufacturer involved in medical devices willing to know more about different sterilisation methods and biocompatibility tests
You will learn…
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The significance of sterilisation in the process of designing a new medical device
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How to find the most suitable sterilisation method
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Which biological tests should be done in order to demonstrate biocompatibility of a new biomaterial or a new device
