Barco 3D PACS Visualization Software

August 20th, 2008 Editors Radiology

Barco, a visualization technology company out of Kortrijk, Belgium, has released its latest 3D visualization software package, dubbed Voxar 3D, and integrated it with AGFA’s popular IMPAX PACS system.
From the press release:

Voxar 3D has been specifically designed to optimize the ease-of-use and productivity of the daily imaging workflow. It makes advanced visualization accessible on any IMPAX workstation over a standard 100 Mbps hospital network. Voxar 3D also delivers fast loading. With the client-server ‘Enterprise’ version, loading an entire 1000-slice series in full diagnostic quality takes around 10 seconds, while a 2000-slice series takes about 13 seconds. As a tool for daily use, the suite operates effectively with any CT, MR or PET data, even data of sub-optimal quality.
With the introduction of version 6.3, Barco has also put more emphasis on cost-efficiency. Therefore, the new product only incorporates the features and functionalities that are clinically relevant, with a special focus on reimbursable procedures. It makes use of powerful, off-the-shelf server technology and graphics cards, allowing users to benefit from the latest IT advances at the lowest cost. Along with competitive pricing and flexible licensing, Voxar 3D therefore offers a smart way to introduce advanced visualization throughout an enterprise, not just in a reading room.
Voxar 3D 6.3 can be complemented with a full set of clinical applications for specific medical disciplines.
* Voxar 3D VesselMetrix delivers all the necessary tools for quantitative vascular analysis and stent-graft planning of CTA and MRA studies on one easy screen.
* Voxar 3D CardiaMetrix analyzes multi-phase cardiac CT studies and provides 2D, 3D and 4D visualization for quantitative evaluation of cardiac anatomy and function.
* Voxar 3D ColonMetrix is optimized to visualize supine and prone image studies simultaneously in 2D and 3D. DICOM reports are automatically generated on-the-fly as you diagnose.
* Voxar 3D PET/CT Fusion supports the effective interpretation of whole body FDG oncology studies and provides real-time interaction with PET/CT images.

Press release: Barco’s advanced visualization software fully integrated in Agfa IMPAX…

Upcoming conferences

october

18octallday19alldayWorld Congress on Polycystic Ovarian Syndrome and Fertility, 2018Abu Dhabi, UAE

18octallday19alldayManaging Your Complaints and Obstacles in Post-Market Requirements -- Results from Top Medical Device Observations During an InspectionMinneapolis, MN, USA

Event Details

Post-Market activities, Complaint Handling, MDRs, and Recalls are expensive, time consuming, and often lead to more serious financial consequences. Over 80% of FDA Inspection target observations for lack of compliance in these areas.

By attending this seminar, you will discover:

How to overcome one of the biggest obstacles device manufacturers face
How the FDA expects you to develop and implement proper handling of complaints reportable or non-reportable, product complaint handling and documentation
How and when to file Medical Device Reports (MDR), effective and appropriate communication with the appropriate regulatory agencies in the event of a recall.
How to conduct a correction and removal actions to avoid a recall crisis, including required recordkeeping, expectation from FDA and other regulatory agencies in the event of a recall and key factors in implementing and maintaining compliance with the regulations and real life experiences of FDA.

**New course materials have been added, updated content will include:

Creating Standard Operating Systems (SOPs) for Post-Market Quality Systems and
What to expect from the changes in ORA with Inspection Structure Realignment

This Seminar will have you stop spinning your wheels with nonessential activities, and leave you with a comprehensive learning package that only Rita Hoffman, a former FDA CDRH Recall Branch Chief with experience across the device, drug and veterinary industries can provide.

Spend one and a half days in an interactive course led by Ms. Rita Hoffman, Former FDA CDRH Recall Branch Chief with over 36 years with FDA and leading Industry Expert, who will provide the participants with tools to minimize risk of regulatory enforcement actions.

Time

october 18 (Thursday) - 19 (Friday)

Organizer

Compliance Online 80068SEM

Learn More

Calendar GoogleCal

18octallday19allday18th Global Ophthalmology, Optometry and Glaucoma Conference, 2018Helsinki, Finland

18octallday19alldayBiology and Pathology of Infectious Disease Conference, 2018Helsinki, Finland

18octallday19allday14th Global Biomarkers Summit, 2018Amsterdam, Netherlands

22octallday23alldayInternational Conference on Breast Cancer, 2013Vancouver, British Columbia, Canada