AI in intensive care: cooperation between an SME and a Piedmontese start-up
2023-02-06 14:30 - 15:30 (Europe/Rome) | Online
We start from the experience of an SME and a start-up of the territory to deepen how artificial intelligence can be a key element for the development of the healthcare sector.
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Webinar goals
The webinar will provide an overview of the activities of the two companies, in cooperation with each other, engaged in the improvement and decision support to the clinician, especially for intensive care. Taking as an example a clinical problem, we will examine how we can realize innovative technological solutions both software and hardware to assist clinicians and get effective predictors able to support the doctor in critical decisions.
Target group
SMEs and start-ups, operating in the healthcare sector.
What we learn from the webinar

Elements of the process of development of technological innovations in healthcare
How artificial intelligence can be applied in the healthcare sector and in particular within intensive care departments
Experiences of an academic technology transfer path: from the patent to the start-up
Applied research: development of a prototype from TRL4 to TRL7
The benefits of the supply chain: Research organisation – Start-up – SMEs

Program

Experience in creating digital-health start-ups in Italy
Process of creating an innovative new product in healthcare

Lecturers

Andrea Ancona. Administrator of digital health start-up U-Care Medical and co-founder. Coordinates the activities of the enterprise, sets the business strategy and technological development. Following his Master’s Degree in Micro and Nanotechnology, he obtained a Doctorate in Physics from the Polytechnic of Turin. Subsequently, he worked for 2 years in the Area for Technology Transfer and Business Relations of the Politecnico di Torino, and obtained an Executive MBA from the School of Management of Trieste. He is the author of 4 patents filed, 13 scientific articles in international journals and coordinated fundraising activities for a total of about 1M €.
Davide Capello. R&D Manager and co-founder of SME Novasis Innovation. After graduating in Physics in 1999, he specialized as a designer of electro-optical devices at the Fiat Research Centre. He works in the groups of Innovative Product Technologies, Micro and Nanotechnologies and Process/Product quality, as R&D Project Manager. He has participated in more than 20 collaborative, regional and European research projects, and over the years has held the roles of Project and Workpackage Manager. Since 2012 he has carried out fund raising, project management and coordination activities for R&D and product development in Novasis Innovazione. Since 2017 he has been an expert for the evaluation and review of regional and European research projects. He’s the author of five publications and five patents.
Valentina Cauda is Prof. in Experimental Physics at the Politecnico di Torino. After a degree in Chemical Engineering in 2004 and a PhD in Materials Science and Technology in 2007, she did several research periods abroad, in particular at the Complutense University in Madrid and at the University of Munich where she spent three years as a researcher working on nanoparticles for the controlled release of drugs. From 2010 to 2015 she returned to Italy as a post-doc researcher at the Turin office of the Italian Institute of Technology, then obtaining a position as Associate Professor at the Politecnico di Torno from 2016 and working in the field of nanomedicine. For his research he has received several awards and awards. She is the author of 140 publications in international scientific journals, 7 international patents and winner of numerous national and European funding, including the most prestigious European Research Council project ERC Starting Grant (TrojaNanoHorse) from 1.5 million euros.

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Tax credits for companies investing in innovation
2023-02-23 11:30 - 12:30
What tax breaks are ideal for improving the competitiveness of businesses and making them grow? What does Patent Box mean? What does the relevant legislation say in terms of facilities? These are just some of the questions we will answer in the dedicated webinar.
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Webinar goals
The focus of the webinar is to address the issue of tax concessions aimed at supporting the competitiveness of businesses.
In detail the following three tax advantages will be treated:

Tax credit Research, Development and Technological Innovation – objective: to stimulate investment in R&D, technological innovation, also within the 4.0 paradigm and the circular economy.
New Patent Box – objective: Optional scheme to increase expenditure
supported by the enterprise in relation to copyrighted software, industrial patents, designs and models.
Capital Goods Tax Credit 4.0 – objective: to support and encourage companies that invest in new, tangible and intangible capital goods, of a 4.0 character, functional to the technological and digital transformation of production processes.

Target group
To all holders of business income, regardless of the legal nature, size and production sector to which they belong.
What we learn from the webinar
It will be possible to deepen the reference legislation in relation to the three preferential products: objectives, beneficiaries, eligible investments, eligible expenses, reference rates, access requirements, etc.
Program

Overview of the state of the art of Tax Credit Research, Development and Technological Innovation;
Patent Box;
Capital Goods Tax Credit 4.0.

Lecturers

Introduction: MARIA CRISTINA GIACOBBO SCAVO – CHIEF EXECUTIVE OFFICER VALUE SERVICES SPA
Overview of the state of the art of the Tax Credit Research, Development and Technological Innovation: GENNARO ERRICO – OPERATIONS MANAGER VALUE SERVICES SPA
New Patent Box: MARIA CRISTINA GIACOBBO SCAVO – CHIEF EXECUTIVE OFFICER VALUE SERVICES SPA
Capital Goods Tax Credit 4.0: FRANCESCA FERRI – GRANT SENIOR CONSULTANT Q&A VALUE SERVICES SPA

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Medical devices: correct handling of non-compliant model
2023-02-27 14:30 - 15:30
Starting from the general definition of non-conformity of a medical device, we will focus on how to manage a situation of this type, illustrating the process of managing the rework and/or disposal phases.
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Webinar goals

Understand the context of non-conformities within a Quality Management System
Define the non-compliant product
Internalize the flow of the non-conformity management process
Describe the fate and disposal of a non-compliant product
Define the concept of rework of a non-compliant product

Target group
Quality Assurance/Regulatory Affairs of medical device manufacturers and contract medical device manufacturers
What we learn from the webinar
The correct approach to dealing with non-compliant medical device cases
Program

General aspects
Regulatory framework
Control of a non-compliant product
reworking

Lecturer
Federica Carra. Graduated in Chemistry and Pharmaceutical Technology at the University of Turin, she has twenty years of experience in Pharmaceutical Quality Control, during which she obtained recognition for the suitability of a Qualified Person. Since 2016 he has been collaborating with Chemsafe for the design, Development and maintenance of ISO 9001 certification as Quality Manager and in the design and development of quality management systems for manufacturers of medical devices in accordance with current legislation. He is auditor of first and second part of Quality Management Systems GMP, ISO 9001, ISO 13485, ISO 22716, ISO 15378.
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