Hardware design is carried out through a formalized development cycle that includes the following main activities:

• Definition of hardware requirements starting from system requirements, with allocation of functionalities to be implemented in hardware
• Hardware architecture design, including block diagram and selection of electronic components
• Detailed design of individual circuit sections related to topologies, including component sizing and, where necessary, simulations and/or experiments
• Unit verification on prototype of individual circuit sections, under all operating conditions, including fault conditions
• Hardware-software integration and system verification
• Requirements traceability throughout the development cycle
• Configuration management and versioning of all design items
  

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Real-time embedded software development is based on a solid set of paradigms, methodologies, and technologies developed over our years of experience in the field. By applying principles of computer science to embedded and real-time systems, we constantly update our methodologies and technologies to reflect the evolution of electronics, computing, and regulatory context.

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Teoresi MedTech conducts industrial research programs both for clients and on internal projects. The programs aim to acquire new knowledge and skills to be applied to product development. Recognizing the importance of collaboration with universities, Teoresi MedTech actively involves Italian and foreign institutions in its research programs.

Ongoing Research Programs

Demographic evolution requires a reorganization of healthcare services to manage the growing number of elderly individuals and the increased prevalence of chronic diseases. Telemedicine is considered an essential tool to promote a paradigm shift congruent with demographic changes, but various limitations remain for its full adoption, related to issues in design, integration with the healthcare service, and usability by end-users. REMEDY is a new customizable service integrable into the Hub and Spoke healthcare organizational model for remote and multiparametric monitoring of complex and multicomorbid patients. REMEDY will be co-designed with clinical operators, patients, and companies to gather their needs and desires and create a service that can integrate into clinical practice. Specific objectives include designing innovative tools for monitoring, engaging, and empowering patients, developing an innovative wearable and multisensor device, and an Internet of Medical Things (IoMT) platform for the collection and processing of clinical data. REMEDY tools will be engineered, accompanied by technical documentation, and validated in conditions of use similar to the clinical context.

Future of Agricultural Tractors – FACT

FACT envisages the development of a virtual and experimental laboratory dedicated to agricultural vehicles of different types and sizes, for the study of efficient, sustainable, and safe solutions. The goal is to create synergical tools to identify innovative solutions to reduce energy dissipation, improve operator comfort, and accelerate the agricultural machine’s “transition” towards sustainability. The proposed activity involves modeling selected vehicles (tractors, lawnmowers). After experimental validation, the Digital Twin will allow the evaluation of multiple different designs: a difficult, costly, and highly polluting operation if carried out through physical prototyping. In the context of emissions reduction, options for electrification of components will be evaluated, including for equipment. An experimental laboratory will be equipped, a physical platform to validate the effectiveness of proposals identified through virtual analysis. The laboratory will be gradually expanded starting from an existing “embryo,” to build independent equipment available to research centers for experimentally analyzing issues related to the efficiency of agricultural machinery.

Completed research programs

• High performance control solutions for PMSM

• Use of wearable inertial sensors in motor rehabilitation of patients with severe acquired brain injury

• Advanced and innovative human-machine interface design for CRRT device

• Wireless sensor network for advanced industrial and biomedical application

• A novel pump-free ultrafiltration rate modulation system for continuous renal replacement therapy applications 

• Multi-parametric model for estimation of arterial CO2 tension via oxygenator exhaust capnometry in extracorporeal lung support devices

Verification and validation ensure compliance with industry regulations and product quality. The Verification activity consists of confirming, through objective evidence, that the input requirements are fully and correctly implemented. The Validation activity consists of confirming, based on evidence derived from a set of activities, including Verification, Risk Management, Usability Analysis, etc., that the requirements for the intended use are met.
Verification in both hardware and software development cycles involves all project phases: requirements, architecture, implementation, integration. These verifications are supported by tools and automated tests to ensure the accuracy and reliability of the entire process.

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Risk management is a crucial element in ensuring product safety and achieving the necessary certifications. It accompanies all phases of development in our projects at the system, hardware, and software levels, and is a service we also provide to our clients.
During the implementation of risk management, we scrupulously adhere to specific reference standards for various application sectors and geographic areas, ensuring maximum compliance and safety of products and services.

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All our projects are accompanied by a technical dossier, compliant with sector regulations, and ready to be submitted to certification authorities. This service, developed through a decade-long understanding of regulations and industry standards, is also available to our clients, who receive continuous support in both their interactions with certification bodies and in documentation aspects, including preparation and audit phases.