Throughout the duration of the project, we defined the MammoWave specifications, reviewed its development plan and supply chain, expanded our knowledge of the market and regulations, and established a commercialisation strategy. The clinical validation was defined with the key objective of confirming the safety, accuracy and usability of the imaging device to deliver and deploy the conventional screening. During the project, a detailed analysis of the potential business models applicable for MammoWave imaging device has been performed. The Phase 1 feasibility assessment has established that a development plan for the MammoWave imaging device is technically and commercially viable, and that implementation of an industrialisation and commercialisation plan should be pursued. SME Instrument Phase 2 funding could provide the correct amount of funding and support to allow the stated activities to be implemented successfully.