Med Fast Track

Med Fast Track 1

This group includes projects that already have an active start-up or spin-off, with a TRL value of at least 4 for the presented products. The projects will be framed and evaluated to identify the levels of innovation compared to existing competing products, their ability to enter a global market, and the financial requirements necessary to develop an industrial production plan. The projects will be appropriately prepared and presented to investors and/or companies in the biomedical sector.

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THE PROJECT

In the first phase of Med Fast Track, companies will be evaluated based on key areas, such as the innovativeness of the medical device, the identification of needs that will be met by using the device, the market potential, and how structurally ready the company is to enter the market.

CERTIFICATION PROCESS

Step 1

Step 1

Step 2

Step 2

Step 3

Step 3

CONTINUE WITH MED FAST TRACK 2

Clinical investigations on devices refer to scientific studies and trials conducted on medical devices to evaluate their effectiveness, safety, and compliance with regulatory standards before they are marketed and used on patients. The main focus of the project is to align the documentation and regulatory requirements to address both pre-market and post-market studies.Learn more.

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