About Three Palm Software

The principals of Three Palm Software have extensive experience in developing software applications for medical imaging. Our goal is to apply this expertise to the development of innovative, clinically useful software applications.


The mission of TPS is to become the leading developer of screening software for early diagnosis products – including imaging workstations, clinical data collection and analysis, and computer aided detection, specifically designed to aid in the early and accurate diagnosis of diseases at their earliest and most treatable stage.

Company history

Three Palm Software was founded in February 2007 (initially as a LLC) by a small group which has worked for many years in various parts of the medical imaging industry. In April 2008, the company transitioned to a “C” corporation and is now known simply as “Three Palm Software”. In April of 2011, the company opened its second office (in Campbell California) in order to strengthen customer support and training. Subsequently, in October of the same year, the company extended its business from a focus on women’s health to the more general arena of screening for early diagnosis.

Professional experience of the founders

We have previously been employed at several of the key players in the industry, and have developed applications for them and other companies. We have been key contributers to products that have (or are still being) marked by companies such as GE, Siemens, Philips, Hitachi, Toshiba, Kodak, R2 and a number of smaller companies. Our expertise spans the medical imaging domain – including

PACS workstation; reconstruction algorithms for CT (including cone beam); image processing; 3D rendering and display; computer-aided detection algorithms; user interface design; application and enterprise workflow  We have experience in different modalities (including CT, MRI, Ultrasound and Nuclear Medicine) and medical device connectivity (such as DICOM and IHE), and regulations (we have developed products that have received PMA approval, and have participated in FDA and ISO audits). A common thread in our collective experience is the ability to deliver commercial products in a highly technical domain.