The implementation time varies depending on the size of the institution and the modules selected. Typically, a full implementation takes between 3 and 6 months, including configuration, data migration, staff training, and go-live. Our team develops a customized plan to minimize any disruption to operations.

All our systems hold international certifications: ISO 9001:2015 for quality management, ISO 27001 for information security, and ISO 13485 for medical devices. In addition, we comply with FDA, CE Mark, and MDR regulations depending on the type of solution. Our development centers are fully certified.

Yes, we provide interfaces for more than 500 different medical devices and equipment, including laboratory analyzers, imaging equipment (CT, MRI, ultrasound), vital signs monitors, ventilators, pathology equipment, and more. Our technical team assesses your current infrastructure and ensures full integration.

We provide Triple-A Service technical support with 24/7/365 priority assistance. This includes proactive monitoring, preventive maintenance, software updates, incident resolution, and a dedicated team of specialists. Our goal is to ensure continuous operation and maximum uptime for your institution.

Absolutely. Our systems are designed to meet the highest standards of medical data security and privacy, including HIPAA (Health Insurance Portability and Accountability Act) compliance for the U.S. market. We are ISO 27001 certified and implement data encryption, strict access controls, and ongoing audits.