Aims

To explore materials, design and processes for improved decontamination to maximise compatibility with a range of sterilisation techniques, to target inertia within the Medtech industry

Methods

• Materials compatibility and characterisation through literature review, rigorous testing and material evaluation informed by industry input
• Cyclic testing from baseline material characterisation mapping over repeated cycles of decontamination
• Material characterisation will encompass mechanical testing, material composition, metrology and visual properties
• Device design using alternative decontamination and sterilisation methods
• Implementation for improved device re-use working with industry, regulatory and clinical partners