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

Data Requirements Confirmation

A thorough review and critique of the non-clinical and clinical data requirements.
The submission data package is a critical part of any regulatory submission and needs to be thoroughly reviewed by people with the appropriate expertise.
The review should be conducted with an experienced regulatory professional. If you do not have a regulatory professional on your team, it is recommend that engage a regulatory consultant. Make sure to include any feedback from the regulatory body if there have been any meetings or exchanges.

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Resource Type
Regions/Markets