Medtech and digital health for advanced software solutions
We chose NRG Spa as our IT partner to develop tailor made solutions for unique busines needs with customized technology choices.
NRG is an ISO 13485-certified engineering partner with over 20 years of experience in developing complex software systems for medical devices, digital health platforms and clinical applications.
Since years, NRG collaborates with established medical devices manufacturers, startups and research centers to design and develop software solutions that operate in regulated and high critically environments.
NRG teams works directly with clients’ R&D departments, contributing to software architecture definition, systems integration and stabilization of complex technological platforms
A Technology Partner For Medtech Innovators
- Development of certifiable software for medical devices
- Systems integration and interoperability
- DICOM Systems and medical imaging
- Secure architectures and cybersecurity by design
- Long term collaboration with internal R&D teams
- A network of specialized and certified IT partners for mobile solutions, AI applications, HW and FW
Regulated Software Development
Our NRG partner, operates under an ISO 13485-certified quality system and supports software development in compliance with major regulatory requirements, including MDR and FDA. The processes adopted ensure requirements traceability, validatable documentation, and audit readiness throughout the entire development cycle.
Technological Expertise
The key areas where NRG’s performance delivers are:
- Cloud architectures for medical platforms
- DICOM and medical imaging systems
- Connected medical devices and clinical IoT
- Data analysis and AI applications in healthcare
- Advanced interfaces and 3D visualization
Technologies
C# / .NET / Blazor / JavaScript / TypeScript / React Azure / AWS / .NET Aspire PostgreSQL / MongoDB / Redis API REST / GraphQL
Engineering And System Oriented Approach
Each project is approached as a systems engineering challenge.
NRG teams integrate software architecture, interface design, and validation practices to create robust and maintainable solutions over time.
This approach enables support for products that need to evolve while maintaining stability, quality, and regulatory compliance.
Contribution To Regulated Development Processes
Support For Design Control Processes:
NRG directly contributes to development activities within Design Control processes, supporting clients in:
- Defining functional requirements
- Designing software architecture
- Developing and verifying code
- Validation and documentation activities
These activities are carried out in collaboration with clients' quality and regulatory teams.
How R&D MedTEch Teams are going to be supported
Development of New Certifiable Products
Evolution of Existing Platforms
Technical and Regulatory Support
Research and Innovation Activities
Integrated Competence Ecosystem
Integrated Hardware–Firmware–Software Systems
NRG supports the design of complex systems integrating hardware components, firmware, and software platforms.
Mobile Applications as System Extensions
Mobile applications are designed as integral parts of the technological ecosystem of the device or clinical platform.
Cybersecurity by design
Security is integrated from the earliest stages of architecture design, including data, device, and infrastructure protection.
The NRG team acts as an engineering partner for MedTech companies, developing complex and regulated software systems.
The company supports clients' development teams in designing robust architectures, integrating systems, and evolving software platforms for clinical contexts.
Case Histories
- Date
- 16 Gennaio 2023
- Date
- 13 Gennaio 2023
- Date
- 9 Gennaio 2023
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