Risk Management: Best Practices for Medical Device Profitability
FDAnews and Industry Directions Launch New Study
FALLS CHURCH, Va. and CUMMAQUID, Mass., April 23
/PRNewswire-USNewswire/ -- FDAnews and Industry Directions Inc., in close
association with research analysis partner Cambashi Ltd, today invited
medical device manufacturers to respond to a new survey on current industry
challenges and practices. The survey asks about company objectives,
business processes and practices, information systems and applications, and
performance.
The research team is seeking responses from all companies in the
medical device industry -- of all sizes, all classes of devices, and in
every geographic region. The initial online survey is open for industry
response from now until early May. All responses will be aggregated to
formulate report findings. Individual responses will remain strictly
confidential.
The results of this survey will be released at the Fifth Annual Medical
Device Quality Congress June 25-27 in Cambridge, MA in a special session on
the research, Risk Management: Best Practices for Medical Device
Profitability. This research ties in closely with this year's conference
theme, Leading the Way to Better Performance With Quality Systems
Compliance.
The study findings will be used by medical device manufacturers and
others serving the industry to improve their performance and reduce
business risk. The study will assess and identify opportunities for
streamlining practices so manufacturers can achieve quality and regulatory
compliance while increasing profit and growth.
The online survey is available at:
http://www.surveymethods.com/EndUser.aspx?F4D0BCA5F6BEA6A6 or through
www.fdanews.com or www.industrydirections.com. The survey is open to
medical device manufacturers of all sizes worldwide. All survey respondents
will receive a copy of the public findings report when it is released.
The research has been sponsored by five co-sponsor companies -- all of
whom are active in the Medical Device sector. The analysis will be
completed by Cambashi Ltd. and the report will be prepared independently by
Industry Directions, which retains full editorial control.
The five co-sponsor companies underwriting the effort provide deep and
diverse expertise in medical devices practices and provide production,
quality, compliance, document management, and enterprise software to the
industry. These companies are working together to increase the medical
device market's understanding of how to reduce risks and improve compliance
and profitability. Research sponsors for the study are: Camstar Systems
(www.camstar.com ), IBS America (www.ibs-us.com), IQMS (www.iqms.com),
MasterControl (www.mastercontrol.com) and Pilgrim Software
(www.pilgrimsoftware.com).
SOURCE FDAnews
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