Healthcare & Medical Devices
In the healthcare sector, where patient safety and diagnostic reliability are absolute imperatives, electronic excellence is not an option. Every component, every line of code and every manufacturing process must meet the most stringent regulatory standards.
Groupe Synov is the ISO 13485-certified industrial partner that accompanies medtech players from design to production of life-saving and life-enhancing medical devices.
Our response to the requirements of the Healthcare & Medical Devices sector
Our organization is fully structured to guarantee the compliance, safety and innovation required by this market.
- Strict regulatory compliance
Our ISO 13485 certification guarantees a quality management system adapted to the design and manufacture of medical devices, including Class IIa, IIb and III. We ensure full traceability and the compilation of regulatory technical files. - Design for active and connected medical devices
We design the electronic architectures of complex systems: implants, stimulators, infusion pumps, biomedical sensors and e-health devices, integrating the constraints of miniaturization, biocompatibility and data security. - Lifecycle and obsolescence management
The long lifespan of medical equipment calls for proactive risk management. We offer maintenance, requalification and component obsolescence management services to ensure the long-term durability and safety of your devices.
Our core competencies
Design and industrialization of ISO 13485-compliant medical devices.
Integration of secure connectivity solutions for e-health and patient monitoring.
Manufacturing in a controlled environment (clean room on request).
Maintenance and lifecycle management of critical products.
Fields of application
Active medical devices (class IIa, IIb, III)
- Implants ;
- Stimulators ;
- Pumps.
Connected healthcare solutions
- Battery management ;
- Conversion.