Standards Commitment

All of Pro Medicus’ wholly-owned subsidiary, Visage Imaging – Visage 7 products are based on open standards like DICOM and HL7 in order to provide the best possible interoperability with imaging informatics and healthcare information systems, such as, but not limited to, RIS, PACS, EHR, VNA, Workflow Platforms, Analytics Platforms and Reporting Systems.  In our experience, commitment to open standards results in proven, reliable integration.

Pro Medicus’ wholly-owned subsidiary, Visage Imaging, also supports the Integrating the Healthcare Enterprise (IHE) initiative and is certified for numerous integration profiles.

Please be advised that Visage RIS is not a medical device.

Conformance Documentation

pdf DICOM Conformance Statement – Acrobat pdf 956k

pdf HL7 Interface Specification – Acrobat pdf 811k

pdf IHE Integration Statement – Acrobat pdf 15.9k

pdf Symbols for Proper Use– Acrobat pdf 48.7k

Quality System and Product Quality

All processes at Pro Medicus’ wholly-owned subsidiary, Visage Imaging, are oriented towards maintaining superior product and service quality for the benefit of our global customers.  Internal and external audits guarantee continuous monitoring and improvement of our quality management system.  Consistent with our company philosophy, all of our employees are challenged on an ongoing basis to contribute to the continuous improvement of our products, services, and processes.

Our customers can rely on Pro Medicus’ wholly owned subsidiary, Visage Imaging, complying with the relevant international quality standards – confirmed every year through certified regulatory bodies.  Our quality management system complies with:

pdfISO 9001:2008 – Acrobat pdf 491k

pdfISO 13485:2003 – Acrobat pdf 768k

pdfISO 13485:2012 / AC:2012 – Acrobat pdf 99k

pdfCanadian MDR Regulations CMDR License 72841 – Acrobat pdf 237k

pdfAnnex II of the European MDD 93/42/EEC – Acrobat pdf 110k

FDA QSR – 21CFR820 (U.S.)

In addition to these international certifications, the Visage 7 product line has received 510(k) clearance to market from the FDA and is also registered as medical device in Europe, Canada and Australia.

This underscores our dedication to manufacturing, marketing, and supporting only the highest quality products and medical devices for the global market.