SenesiaHC is specialized in Medical Diagnostic Software development. We deal with software design and development for diagnostic systems & medical devices. We have 15 years experience in software solutions for diagnostic companies, medical and healthcare start-ups. Our mission is to develop software focused on the user’s experience and requirements, allowing companies to save time and money.
Software development for medical diagnostic systems
We design & develop agile
custom-made software for
medical diagnostic producers
An exceptionally software tailored to you
Standard-compliant software development:
IEC 62304:2006 for medical software development;
Food and Drug Administration’s (FDA) Content of Premarket Submission for software Contained in Medical Devices.
Our software engineers develop software solutions that enhance the “user experience”: software that improves the usability of the diagnostic systems, favoring its easeness of use and interaction with the user.
Our philosophy is to support the client throughout the product life cycle: we are aware that software needs continuous technical and
security updates. We are constantly in touch with our customers, guaranteeing continuous technical assistance with releases and new updates.
Our Staff is able to develop “agile” software, available in short time: our software are “taylor made” solutions that are implemented with the customer, in order to identify/cover any needs and requirements.
Our Company adopts a “circular approach” to software development: during the prototyping process the customer has an important role in the validation of the final product
Software Development Process
A circular approach to software development
The first step concerns the software development process: the design of the software architecture, with the list of hardware and software components.
The first step begins with a meeting with the client company to understand their needs.
- the functions that the user needs
- the hardware features.
After this meeting the “first requirement document” will be provided, which will be subsequently updated. At the same time a document will be prepared with guidelines on software development to standardize the functional and graphical features of the user interface. Based on the first requirement document, possible risks associated with the use of the software/hardware are evaluated in order to develop a reliable software architecture.
The second step deals with the software design, the technology to use, the feature of the hardware components.
This phase is dedicated to:
- reduce the development time of new features
- facilitate the software maintenance
- get high quality graphic design standards
- maximize the software usability.
During the third step, product tests and usability tests are organized to verify the software “easiness of use”.
SenesiaHC adopts a “circular approach” to software development where throughout the development process the customer continuously validates the product.
Standard- compliant software development:
We develop software to insure full-compliance with:
- IEC 62304:2006 for medical software development
- Food and Drug Administration’s (FDA) Content of Premarket Submission for Software Contained in Medical Devices.