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To: Carl Worth who wrote (27251)12/30/2004 8:40:52 AM
From: GARY P GROBBEL  Read Replies (1) | Respond to of 120415
 
CMPD Carl...this is the plan for the OsteoGram and many parts of it are already underway..and their proress on same is why i think 2005 will be the year they make real headway:

During fiscal 2003, we altered the strategic direction for the OsteoGram(R)
product, and throughout fiscal 2004 we implemented our new strategy. We believe
that the future of our OsteoGram(R) technology is in the development of medical
software applications for digital (filmless) imaging equipment, which is a high
growth segment of the medical imaging field. The Digital Communications and
Imaging in Medicine (DICOM) standards-based version of the OsteoGram(R) is our
first product in this emerging arena. Although we believe that the underlying
technology for the OsteoGram(R) can be applied to disease states beyond
osteoporosis, we continue to maintain our focus on the manageable market segment
of this bone disease. Our research and development team devoted the majority of
their time this fiscal year becoming skilled at integrating our software
application into several digital imaging platforms. As our knowledge base
increased, we have become more adept at the integration process, and we expect
to adapt our software to many more DICOM platforms in fiscal 2005. We also
expect that numerous licensing agreements for our software will come to
fruition, as imaging equipment manufacturers realize the value of placing an
added reimbursable procedure for a prominent disease onto their workstations. A
derivative of our integration efforts is the design and development of two new
OsteoGram(R) products, the OsteoGram CADKit and the OsteoGram CADServer , both
of which are add-on hardware for digital imaging equipment and networks. These
products will house the current OsteoGram(R) software plus our future
applications for arthritis, scoliosis, vertebral fracture assessment and
software for screening osteoporosis on digital mammography equipment. We have
also expanded our international distribution through country-specific
distributors, and as we conclude the requisite work for obtaining our CE Mark,
our distributors are preparing to launch the OsteoGram(R) in their respective
countries. A CE Mark is the regulatory approval for the European Union and its
related countries.

Our efforts in the international arena continue. Rather than build our own
global sales force, we use existing distribution channels that include a mix of
manufacturers' direct sales representatives and local distributors. During
fiscal 2004, we added distributors in the United Kingdom, Czech Republic, Italy,
Benelux, Austria, Pakistan, and Croatia. Our distributors in the European Union
are awaiting the issuance of our CE Mark to initiate sales, and we
anticipate their contribution. The member countries to the European Union are
of particular interest, since their conversion to filmless x-ray systems is far
ahead of the U.S. market. In order to enter the European Union we will need to
have a CE Mark, indicating that we have conformed to all the regulatory
obligations required by European Union legislation. We expect to complete this
process in early fiscal 2005. The Chinese market has been a disappointment in
fiscal 2004. We experienced a slowing of sales for our older, film-based unit;
however, we laid the groundwork for the introduction of our DICOM version of the
OsteoGram by expanding distribution to include Siemens AG, Orex's local partner.
In addition, we installed two prototypes of our new OsteoGram CADKit in hospital
accounts in China. The units are functioning well and customer satisfaction is
at a high level.