Here you can download our press releases in the PDF file format. You will need the latest version of Adobe Reader to view these files. This is a free download.
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Prowess Inc. Announces FDA 510(k) Clearance for PUMA (OIS | R & V) |
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July 07, 2010
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Concord, CA, June 2010 – Prowess Inc, a radiation oncology treatment-planning software company, has received FDA 510(k) clearance for Puma (Oncology Information System | Record and Verify). Offered at an enticing price, Puma is so affordable that medical professionals will be able to acquire a new OIS | R&V system for their oncology department without the typical anxiety over how to meet a tight budget.
Prowess created Puma to provide a comprehensive and highly reliable computerized Record and Verify System to help radiation therapists improve quality control and provide invaluable scheduling, record-keeping, and report-generating functionalities. Fully integrated, Puma enables a paperless office by importing radiation treatment plans in DICOM and RTP. The result is an intuitive system that expedites the clinical workflow and empowers the oncology team to focus on their highest priority – the patient.
Key Features and Benefits:
• Oncology specific EMR
• Diagnosis and Staging
• Radiation prescription monitoring
• Scheduling and Reports
• Simple, Intuitive Interface
• HIPAA compliance
• Multi-client access to central database
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DAO/IMRT Product Technology Moves Closer to Perfection |
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July 20, 2009
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We are excited about our first MU effective Direct Aperture Optimization (DAO) based Treatment Planning System (TPS); we continue to incorporate higher standards to improve Clinical treatments. Prowess continues to review advances in research and technology that would enhance the performance of its products to increase patient benefits. |
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Prowess Announces 510(k) Clearance and Release of RealART. |
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May 29, 2009
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Radiation Oncologists now can offer treatments customized to the patient’s anatomy right before treatment to target the tumor and spare healthy tissue.
Concord, CA, May 2009 – Prowess Inc. has received FDA 510(k) clearance for RealART (Real-Time Adaptive Radiation Therapy). With this latest innovation Prowess demonstrates
their commitment to Research and Development as well as offering continuous improvement to the radiation oncology treatment field.
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Prowess Announces Release of Version 4.6 for December. |
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December 15, 2008
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New release achieves superior IMRT plans in minutes.
Concord, CA – Prowess, INC. has proudly announced the release of the latest version of their treatment planning system, Panther Version 4.6, for December 2008. Among its other noteworthy technological advances, this version’s greatest improvement is in the speed of IMRT Optimization and quality of plans it generates.
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Siemens Healthcare Announces Exclusive Partnership With Prowess Inc. |
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February 20, 2008
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CONCORD, Calif., Feb. 20 /PRNewswire-FirstCall/ -- Siemens Healthcare (http://www.usa.siemens.com/healthcare) announces an exclusive partnership with Prowess Inc. to develop advanced radiation oncology treatment planning software for integration into Siemens' linear accelerators. The combination of Prowess' unique treatment planning system with Siemens' leading oncology solutions technology will help provide users with one of the most effective and reliable radiation therapy treatment solutions available in the market.
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