Electronic Quality Management System (eQMS) for Medical Devices
Optimize Quality and Regulatory Compliance for Medical Devices
In the highly competitive medical device industry, maintaining a robust quality management system is essential to comply with regulations and ensure patient safety. Our Electronic Quality Management System (eQMS) is specifically designed for the medical device sector, simplifying the implementation and maintenance of standards such as ISO 13485.
Key Benefits of Our eQMS
- Automated Regulatory Compliance
Keep your company aligned with current regulations, including Regulation (EU) 2017/745 (MDR), applicable to medical devices. - Centralized Documentation
Manage all quality-related documents on a single platform, ensuring accessibility and version control.
- Efficient Processes
Automate critical workflows such as non-conformity management and corrective actions, reducing errors and increasing efficiency.
- Simplified Audits
Facilitate internal and external audits with complete and easily accessible electronic records.
Outstanding Features
User-Friendly Interface
Designed for quick adoption by your team, minimizing the learning curve.
Data Security
Advanced protection for sensitive information, complying with the highest security standards.
Scalability
Adaptable to the needs of companies managing medical devices at various stages of growth.
