Healthcare Innovation Cycle for "MedTech" Solutions

MedTech is broad term for electro/mechanical medical devices. Tracking data has been added to show an example of an early stage team at risk due to a focus on technology. Select any Maturity Level to see the core Requirements or select the Requirements themselves to see a description of what is involved in completing a requirement and curated resources.

Note:To access the Resources that describe each Deliverable, use the Sign-in button above to create an account and then click on the Deliverable or the Innovation Maturity Level to see all Deliverables at that level and click on the one of interest.

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checklist.

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MaturityDisplay

Requirement

Institutional Approval Request(s)

A justification and proposed protocol for testing your solution with patients at an institution if clinical data is required.
In cases that require clinical data, institutional groups (i.e. IRBs) approvals are necessary to conduct your studies and represent another source of validation for your idea. Even if the regulatory bodies do not require it, check with potential funders to see if they will require proof that the solution provides economic value in the intended setting.
Follow the rules established by your institution.

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Resource Type
Regions/Markets