Do you have much engagement with the third sector who might be able to co-fund and, certainly, provide access to patients and carers?
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Does i4i fund digital technologies and if so what type of technology do you favour?
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Are the team happy to deal with late stage studies such as comparative device studies or do you concentrate on early feasibility work?
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Is your laser technology for use by a Dr or can it be used by a nurse?
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What proportion of your IIT are focused on evaluating a medical technology?
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Does SBRI application require an NHS partner or is possible for businesses to apply before these links are established?
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Does this mean that all currently CE marked devices will need to undergo a UK CA approval process or would they be adopted into the UK CA?
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What will companies need to do where they already have a CE Mark?
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Are companies more likely then to only get CE marking for the wider European market rather than CA marking just to access the UK Market?
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