Yes, iQ-VIEW supports GDPR (DSGVO) compliance requirements for handling patient data and medical imaging information within healthcare organizations. The system includes features that support secure data handling, controlled access, and medical data protection workflows in compliance with European privacy regulations. GDPR-compliant functionality helps healthcare providers protect sensitive patient and diagnostic imaging data.

Yes, IMAGE Information Systems Europe GmbH operates a certified quality management system according to EN ISO 13485. This certification demonstrates compliance with internationally recognized quality standards for medical device manufacturers and healthcare software development. ISO certification supports high-quality product development and regulatory compliance processes.

Yes, iQ-VIEW is part of the iQ-SYSTEM PACS platform and is certified according to the European Medical Device Regulation (MDR). The software complies with European regulatory requirements for medical imaging, diagnostic workflows, and healthcare software solutions. CE certification supports the use of iQ-VIEW within European healthcare organizations and clinical environments.

Yes, iQ-VIEW is part of the iQ-SYSTEM PACS platform, which is FDA cleared for medical imaging and diagnostic use. The system is designed to support professional clinical workflows in radiology, diagnostic imaging, and healthcare environments. FDA clearance confirms compliance with applicable regulatory requirements for medical imaging software.