James Morisson

PharmaLex

James Morrison B.App.Sc. CMatP is qualified in Materials Science. He has worked in product development as a Materials Scientist and Engineer for over 30 years. He has worked in medical device development since 2005, specifically in biocompatibility and toxicology. He has undertaken postgraduate education in toxicology in USA, the Netherlands and Turkey.

James has served since 2013 as Australian accredited expert to ISO Technical Committee 194 which is the committee responsible for the ISO 10993 series of standards. He sits on the Standards Australia HE-30 mirror committee responsible for national input into ISO 10993. He is the previous Australian Head of Delegation to ISO/TC 194. He has most recently been an active participant as technical expert and member of drafting committee on current revisions of ISO 10993-17 and ISO 10993-18. He is also the Convenor of ISO/TC 194/WG 5 Cytotoxicity. He also serves as task force member to ISO/TC 121 for development and revision of ISO 18562 series, Biocompatibility evaluation of breathing gas pathways in healthcare applications. This series of standards provides a detailed vertical standard in the lung ventilation area.

James consults to the medical device industry on biocompatibility, toxicology, risk management, product development and regulatory strategy.

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