Services
We work with you throughout all the steps of the innovation pathway.
At Viromii we break down your research results to understand how they fit in the market and how to create commercial value from them.
We achieve this by using many analyses including: market quantifications, application area analyses, competitors and business model analyses, patent portfolios analysis, etc.
We focus on the commercial part of the technology transfer process, which usually is the one that demands the most time and commitment.
For this, we work on matching the research results with the companies that have the potential of bringing them to the market.
We prepare the commercial brochure, identify potentially interested companies and their contact information, and we contact them to extract as many answers and meetings as possible.
Having a clear regulatory roadmap is key for successfully developing life science projects. They are required for securing investment, licensing a new development, defining the next product development steps, etc. Our regulatory roadmaps offer a detailed view of the next steps, tests and assays that your medical device will require to successfully reach the market.
Together with the identification of key issues such as applicable GSPR, harmonized standards or notified bodies (among other items), a useful estimate of times and costs is always included.
Our roadmaps are specifically designed to fulfil the needs and adapt to the limited resources of researchers, Start-ups, and Spin-offs.
Viromii wants to share its knowledge about valorization and tech-transfer with the world.
This is the way for creating a richer society that can take advantage of the full value of its inventions.
That is why, at Viromii, we offer tailored training about these topics to all kinds of research institutions and companies.
At Viromii we break down your research results to understand how they fit in the market and how to create commercial value from them.
We achieve this by using many analyses including: market quantifications, application area analyses, competitors and business model analyses, patent portfolios analysis, etc.
We focus on the commercial part of the technology transfer process, which usually is the one that demands the most time and commitment. For this, we work on matching the research results with the companies that have the potential of bringing them to the market.
We know that the term tech-transfer includes many responsibilities and steps, from administrative paperwork, to technology identification and meetings with researchers and policy makers.
We prepare the commercial brochure, identify potentially interested companies and their contact information, and we contact them to extract as many answers and meetings as possible.
Having a clear regulatory roadmap is key for successfully developing life science projects.
They are required for securing investment, licensing a new development, defining the next product development steps, etc. Our regulatory roadmaps offer a detailed view of the next steps, tests and assays that your medical device will require to successfully reach the market.
Together with the identification of key issues such as applicable GSPR, harmonized standards or notified bodies (among other items), a useful estimate of times and costs is always included.
Our roadmaps are specifically designed to fulfil the needs and adapt to the limited resources of researchers, Start-ups, and Spin-offs.
Viromii wants to share its knowledge about valorization and tech-transfer with the world. This is the way for creating a richer society that can take advantage of the full value of its inventions.
That is why, at Viromii, we offer tailored training about these topics to all kinds of research institutions and companies.
Are you interested?
email us!