Medical devices and pharmaceutical products can present a risk to patients by way of exposure to substances present in manufacturing or packaging materials. This webinar, presented by Craig Donald and Malcolm Rose, discusses how to understand and evaluate those risks by following the procedures set out in ISO 10993.
Topics include extraction options, approaches and subsequent analytical methods as well as various other considerations required when planning such a study. Leachables is another important related topic that is also covered.
This webinar recording will be of interest to medical device manufacturers or pharmaceutical suppliers who wish to understand the toxicological risk from your product's associated materials.
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