Aramark CTS moves to expanded facility; ECRIs healthcare standards directory
available; FDA seeks comments on device user fee program
Aramark CTS Moves to Expanded Facility
Approximately five months after closing on its acquisition of Premiers Clinical
Technology Services (CTS of Charlotte, N.C.) business, managed services provider Aramark
(Philadelphia) was planning to move all CTS employees and operations into a new facility,
still in Charlotte.
A birds-eye view of the Twin Lakes Business Park plant that is
the new home of Aramark CTS.
Located in the Twin Lakes Business Park, the new 90,000-square-foot plant triples the
30,000-square-foot space in two separate locations that Premier had allocated to CTS.
The new location will house executive management resources, business development,
contract management resources and a technical resource center for Aramark CTS.
One hundred percent of the employees who worked for Premier in CTS in Charlotte
are still working for Aramark CTS, said Bob Doster, president, Aramark CTS, formerly
senior vice president, Premier CTS. Were not laying people off; were
actually adding people. There will be more people working in Charlotte than when Premier
was sold to Aramark.
ECRI's Healthcare Standards Directory Available
The Healthcare Standards: Official Directory, 2003 edition, is available from
ECRI (Plymouth Meeting, Pa.).
Meanwhile, for the first time, subscribers to the 2003 print publication also are able
to access ECRIs Web-accessible Healthcare Standards (HCS) Online at www.ecri.org.
The annual directory, now in its 15th edition, carries approximately 36,000 new and
updated titles of healthcare standards, clinical guidelines, and U.S. federal and state
laws and regulations from more than 1,200 organizations in the United States, Canada, the
United Kingdom, Europe, Australia and Southeast Asia.
For copies of the 2003 Healthcare Standards publication contact ECRI by mail at 5200
Butler Pike, Plymouth Meeting, Pa., 19462-1298; by phone at (610) 825-6000, ext. 5891; by
fax at (610) 834-1275; or by e-mail at communications@ecri.org.
Price is $545, plus shipping and handling.
FDA SEEKS COMMENTS
ON DEVICE USER FEE PROGRAM
The FDA has established a public docket to collect comments on the implementation of the
Medical Device and User Fee and Modernization Act of 2002. To see the Federal Register notice announcing the public docket, go to http://a157.g.akamaitech.net/7/257/2422/14mar20010800/
edocket.access.gpo.gov/2003/pdf/03-2604.pdf.
To submit electronic comments, go to http://www.fda.gov/dockets/ecomments.
FDA CLARIFIES 510(k) FEES
The FDA is clarifying its policy regarding rates and interim procedures for medical device
user fees for fiscal year 2003.
The agency said its previous announcement was
inadvertently published with confusing language regarding the fee that must be paid
by a small business that submits a 510(k) premarket notification for FDA review this
fiscal year. The correct policy is that all 510(k) applications submitted in FY03 are
subject to the standard fee of $2,187.
Additional information is available at http://www.fda.gov/cdrh/mdufma. |
AFSMI to Present EZe-Learning to Members
The Association for Services Management International (AFSMI of Ft. Myers, Fla.) recently
entered into a partnership with management and technology consulting firm Vivoconcepts
(Ft. Lauderdale, Fla.).
Under the terms of the agreement, AFSMI will use and market Vivoconcepts
EZe-Learning product, a Web-enabled, client-server-based learning suite.
AFSMI will use EZe-Learning to create accredited continuing education courses for its
members. AFSMI also will market EZe-Learning, to its international members for their own
organizational training needs at a special member price. Currently, EZe-Learning is
available in eight languages.
Fluke Offers Calibration Procedures, Training
Fluke Corp. (Everett, Wash.) introduces new Met/Cal Plus V 7 calibration
procedures for three of its precision Tektronix oscilloscope series.
At the same time, the company is announcing its 2003 calibration and metrology course
schedule for U.S. locations.
The automated Met/Cal Plus V 7 procedures allow technicians to conduct their own
verification procedures on the TDS 5000 Series, the TDS 6000 Series and the TDS 7000
Series oscilloscopes.
Fluke says the procedures reduce performance-verification time to approximately 60
minutes a substantial reduction in downtime, according to the company.
Clinical Dynamics Unveils SmartSat Upgrade
Clinical Dynamics Corp. (Wallingford. Conn.) recently upgraded its SmartSat Pulse
Oximetry analyzer with software and accessories for testing a new Nellcor (Pleasanton,
Calif.) product.
The software upgrade, version 3.08A, and the new Nellcor OxiMax Simulator Cable,
provides Nellcor and other customers with the capability to test Nellcor OxiMax pulse
oximeters and OxiMax pulse oximeter probes. As with all Clinical Dynamics test
equipment, this newest release includes the companys three-year parts and labor
warranty.
Customers interested in upgrading their SmartSat analyzers should have the serial
number of their analyzer handy when contacting the company. Call, toll-free, (800)
247-6427, ext. 210, or (203) 269-0090, ext. 210, for international customers; fax Clinical
Dynamics at (203) 269-3402; or e-mail service@clinicaldynamics.com
Axeda Adds Usage
Application to DRM Product
Axeda Systems Inc. (Mansfield, Mass.) in January announced the latest component
of its device relationship management (DRM) software and services the Axeda Usage
application Axeda Usage enables original equipment manufacturers (OEMs) and their service
providers to use the Internet to remotely monitor, manage and service their devices
without involving the customer. The application
remotely collects data from devices through the Axeda DRM system on a predefined schedule.
The Axeda Usage rules engine then processes the data and compares it to specified
conditions such as previous values, averages, expected minimum and maximum targets, and
more. Based on results, the system triggers notifications to personnel or to business
applications. |
Service in Space
Sound may not travel in the near-vacuum of open space, but on board the
International Space Station (ISS), sound not only makes itself heard, it is considered
comforting and familiar for the crew. Some sounds come from the omnipresent plumbing,
wiring and mechanical hardware; the whir of air-circulation fans, the hum of electric
motors and the switching sounds of pumps going on-off-on-off imbue the ISS with its own
bit of personality. Other sounds, however, are the sounds of service as in
maintenance on health and fitness equipment.
In this October 2002 photo released by NASA in January, ISS Expedition Five mission
commander and cosmonaut Valery G. Korzun (left), and Expedition Five flight engineers
cosmonaut Sergei Y. Treschev and astronaut Peggy A. Whitson perform maintenance on the
Treadmill Vibration Isolation System (TVIS) in the Zvezda Service Module. Korzun and
Treschev represent Rosaviakosmos.
CDRH Aims to Shorten PMA, 510(k) Reviews
Speeding device reviews will be a top goal for the Center for Devices and Radiological
Health (CDRH) in coming years, according to a recent FDA report. The center has set a goal
of issuing decisions in 320 days for 80 percent of premarket approval (PMA) applications
received in fiscal year 2006. In fiscal year 2007, that goal will rise to 90 percent of
PMAs.
CDRH also pledged to revise its PMA filing guidance to more clearly define criteria for
filing PMAs so that fewer incomplete applications will be submitted. In addition, the
center plans to develop more special control guidances to communicate clearly the
regulatory requirements and scientific information expected in premarket submissions.
20,000 Predicted to Attend HIMSS 2003
More than 20,000 healthcare professionals were expected to attend the 2003 Health
Information and Management Systems Society (HIMSS of Chicago) conference at the San Diego
Convention Center, Feb. 9-13.
In the exhibit area, more than 600 vendors were scheduled to display their latest IT
products and services.
HIMSS 2003 also marks the fourth year of the Integrating the Healthcare Enterprise
(IHE) initiative with the Radiological Society of North America (RSNA of Oak Brook, Ill.).
At this point, the collaboration to develop cohesive interfaces between different
information technology systems within the healthcare industry is expanding beyond
radiology, demonstrating the progress being made by IHE towards integration.
Agfa HealthCare (Ridgefield Park, N.J.) will demonstrate its integrated RIS/PACS
software, which Agfa currently is tailoring for Agfa Impax PACS in North America. The
software is designed to include privacy and security enhancements, billing features and
language.
New Program Assesses Field-Service Performance
ServicePower (Annapolis, Md.) and Blumberg Associates Inc. (BAI of Fort Washington, Pa.)
announce a consulting program that assesses field-service performance.
Called the Optimization Impact Study Program, the program enables service executives to
evaluate their organizations field-service performance against industry benchmarks.
By creating a simulation of a companys service business based on real-world data,
the program also measures gains in productivity and customer service via optimization
software.
USCS Renews MedAssets, NCHN Contracts
Capital asset management firm USCS Equipment Technology Solutions (Brookfield,
Wis.) recently extended its working relationships with two long-term customers.
USCS and GPO (group purchasing organization) MedAssets HSCA Inc. (St. Louis) in
December 2002 renewed their preferred-provider relationship for an additional three years.
According to their agreement, USCS provides its Lifecycle Managed Maintenance Program and
Equipment Acquisition Resource to MedAssets HSCA members.
CORRECTION
The Biomedical Association of Southeastern Wisconsin (Milwaukee) addressed the topic of
PACS training at a recent meeting but does not offer monthly PACS seminars. |
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