Yes, iQ-4VIEW 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.

Yes, IMAGE Information Systems Europe GmbH operates a certified quality management system according to EN ISO 13485. This certification demonstrates compliance with international quality standards for medical device manufacturers and healthcare software development.

Yes, iQ-4VIEW 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 and healthcare software solutions.

Yes, iQ-4VIEW 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.