Bleepa achieves CE Mark - Raising the bar for medical communication platforms

About Feedback Medical

Feedback Medical is a specialist technology company providing innovative software and systems to benefit those working in the field of medical imaging. Our products advance the work of radiologists, clinicians and medical researchers by improving workflows and giving unique insights into diseases, such as cancer.

We have over 15 years’ experience in the medical imaging sector and work with customers globally from our headquarters in London, UK. Our products originate from developments by professionals working in real-life medical environments and have been advanced in close cooperation with researchers, radiologists and healthcare IT specialists to ensure user confidence and relevance in today’s medical world.

Our Technology

Our proprietary technologies are Bleepa® , a secure instant messaging system which facilitates the sharing of clinical-grade medical images, TexRAD, the quantitative texture analysis tool and Cadran, a picture archiving communication system (PACS).

Bleepa revolutionises clinical communication through the quality of its clinical-grade imaging (drawn directly from the hospital PACS), integration into hospital systems, communications platform and crucially through its inherent clinical safety structure.

The Cadran image platform provides hospitals and research institutes with a comprehensive picture archiving communication system (PACS) for medical images. It equips users with a flexible, convenient and secure platform for image handling from all imaging modalities, such as CT and PET scanners. Cadran Viewer is certified for clinical use and is CE marked for use in the EU.

TexRAD has featured in over 100 academic publications, won numerous awards and is currently used in over 50 prestigious institutions worldwide. We have recently launched TexRAD Lung for analysis of lung cancer which is certified for clinical use and is CE marked for use in the EU.

[Image Reference]


At Feedback Medical we ensure our products and processes are of a high standard and comply with the laws and regulations of the medical device industry.

We produce and manufacture our products within an ISO 13485 Quality Management System (QMS). This certification was recently updated to the latest 2016 version of the standard. Our QMS incorporates the EU requirements for medical device manufacture as well as the needs of U.S Medical Device regulation (21 CFR 820). We have the capability to produce medical image analysis software products that satisfy the needs of 21 CFR 11 and HIPAA.

ISO Certification