Technical Excellence in Regulated Environments
Starting with general hardware and software engineering, Logik supports companies in delivering high-performance technical solutions. With a clear focus on quality, efficiency and sustainability, we build robust systems that prove themselves in everyday operation.
In medical technology, we combine engineering expertise with regulatory confidence. Whether MDR, ISO 13485 or IEC 62304 – Logik stands for compliant, safe and future-proof medical solutions across the entire product lifecycle.
Our Services
Hardware & System Development
- Embedded hardware & electronics
- Sensors, actuators & interfaces
- Test and inspection systems
- Development-related testing (incl. EMC)
Software & IT Solutions
- Agile software development
- Software testing (unit, integration & system)
- Verification & validation (CSV)
- Cyber security
- Interfaces & data flows
Medical Device Development
- Medical device engineering
- MDR/IVDR-compliant implementation
- Embedded hardware & software solutions
- Design verification & testing
Regulatory & Documentation
- Technical documentation (MDR/IVDR)
- Development file (ISO 13485)
- Software documentation (IEC 62304)
- Traceability & evidence management
Medical Device Product Development
Medical technology development is characterized by high quality requirements and extensive regulatory constraints. Key objectives include reliability, precision, ergonomics and full compliance throughout the entire product lifecycle.
As an engineering and development partner, Logik supports companies in creating stationary and mobile systems – from initial concept to series production support.
Compliance & Standards
Our projects follow established medical technology standards and regulations. Quality, safety and documentation are integrated from day one – not treated as an afterthought.