BIA 101 BIVA® PRO is a portable bioimpedance device designed to deliver fast and reliable body composition analysis in both clinical and field environments. Its redesigned enclosure enhances ergonomics, usability, and professional appeal.
It aims to:
– Enable accurate and repeatable body composition measurements
– Support flexible use across clinical and on-field applications
– Improve user experience through ergonomic and intuitive design
NUTRILAB™ PRO is an advanced body composition analyzer developed for hospitals and research settings, providing comprehensive diagnostic support for nutritional and clinical assessment.
It aims to:
– Support early diagnosis of malnutrition and sarcopenia – Provide clear and immediate clinical insights through integrated risk indicators
– Enhance workflow efficiency with an intuitive touchscreen interface
Creanova supported the project across multiple development phases including differentiating the look & feel for medical and premium environments, optimizing usability, and developing a modular architecture adaptable to different use scenarios. All activities were carried out in alignment with the client’s functional requirements, quality standards, and regulatory framework. The main challenge was create a complete new product identity through simplification while maintaining high design quality.
Additional complexities included:
– Developing a removable handle adaptable to different scenarios
– Managing different display sizes
– Ensuring consistency across the product family
“This project has been a wonderful journey that changed our way of showing our technologies to our customers. Creanova has been a real facilitator in the process.”
Michele Petroni
Business Development Manager
Core activities:
– Benchmarking and competitor analysis
– Product architecture and layout optimization
– Industrial design and New Family Look
– Ergonomic development (single and two hand design)
– CMF definition and aesthetic direction
– Cost estimation to support design selection
Outcome:
– Defined product architecture (modular differentiation for hospital and private contexts)
– Improved layout feasibility and manufacturability
Core activities:
– Mechanical engineering of housings and handle
– Surface analysis for high-quality finishing and smooth transitions
– Material selection and compliance (flammability and IP protection)
– Electronic integration and component protection
– CMF validation through POC prototypes
Outcome:
– Validated design and selected final concept
– Defined manufacturing technologies and tooling approach
– Completed usability tests and prototype validation
We optimized the product for serial production, ensuring manufacturability and consistent quality during production.
Core activities:
– DFM and DFA analysis
– Geometry optimization to reduce defects (e.g. weld lines on dark surfaces)
– Iterative refinement with the client
– Mold design and tooling validation
Outcome:
– Industrial-ready components
– Validated design for manufacturing
– Smooth transition to production phase
Creanova supports the production phase by supplying high-quality plastic components.
Core activities:
– Injection molding of plastic parts
– Pad printing for logos and product identification
– Quality control aligned with ISO 13485 standards
Outcome:
– Reliable and scalable supply of plastic components
– Consistent production quality
– Delivery of finished parts ready for client integration
The collaboration significantly improved product usability, design quality, and manufacturability.
Core results:
– Engineering Quality: improved robustness and structural reliability, optimizing component integration.
– Design & Usability: enhanced ergonomics and handling, improving user interaction and workflow efficiency in diverse scenarios.
– Production Efficiency: reduced part count and complexity, increasing consistency and scalability in manufacturing.
Moreover, this project demonstrates Creanova’s ability to manage complex product development processes from concept to industrialization, integrating design, engineering, and manufacturing expertise.
Key capabilities:
– End-to-end product development
– Strong integration between design and engineering
– Industrialization and manufacturing support
– Ability to handle regulated medical environments
Discover how our milestone-based approach reduces risk, ensures regulatory readiness, and accelerates your path to market.