[IEEE-bhpjobs]
[Fwd: FW: Triangle Area Medical Device Industry Seminar Feb 16]
Esther L.
esther-l at mailsnare.net
Fri Jan 21 21:50:54 EST 2005
-------- Original Message --------
Subject: FW: Triangle Area Medical Device Industry Seminar
Date: Sat, 22 Jan 2005 01:12:36 +0000
From:
To: esther-l at mailsnare.net (Esther Lumdsen)
Esther,
FYI and to pass along to those you know working in devices, and device
regulatory issues.
Regards,
Bill.
*Thanks to our sponsors:*
**
<outbind://2/>
*
<http://www.bpmessagecenter.com/~RaleighChamber/click.asp?key=409058&url=http://www.bpstudios.com>*
*Triangle Area Medical Device Industry Seminar & Reception
Wednesday, February 16, 2005
**2 - 5 pm: USFDA Speakers & Interactive Panel Discussion
5 - 7 pm: Reception*
*North Carolina Biotechnology Center
5 TW Alexander Drive, RTP*
*Location Map <http://www.ncbiotech.org/aboutus/directions.cfm>*
**
*$25 per person
*/(Those who register may attend one or both parts) /
/*Hosted by-*/
Wake County Economic Development <http://www.raleigh-wake.org/>
NC Medical Device Organization <http://www.ncmedicaldevice.org/>
Register now to attend the Triangle Area Medical Device Industry
Seminar & Reception, featuring USFDA's Peter Carstensen and Ron
Kaye. They will discuss human factors engineering design standards
for medical devices and other related topics. The event will also
include an interactive panelist discussion and an evening reception.
*Peter Carstensen** *is a senior systems engineer specializing in
human factors for the Center for Devices and Radiological Health
(CDRH) at the US Food and Drug Administration. He has been actively
involved for more than 30 years in national and international
standards writing committees for medical devices where he represents
FDA's interests. He serves on several AAMI, ASTM and IEC and ISO
medical device standards committees dealing with anesthesia and
respiratory equipment and human factors engineering.
*Ron Kaye* is a human factors specialist for the Center for Devices
and Radiological Health at the US Food and Drug Administration. His
work focuses on safety of medical equipment with respect to use
issues including research on device use-safety issues, participation
in national and international standards, and guidance development
and outreach to professional communities and medical device users.
*_Register Online by February 11.
<https://www.wliinc.com/cgi-bin/foxweb.dll/commcale/99Profile?caleid=472&action=register&cc=GRCOC>_**
*/No refunds after deadline./
Questions? Contact John Nelms at 664.7048 or jnelms at the-chamber.org
<mailto:jnelms at the-chamber.org> or Jennifer Murray at 664.7066 or
jmurray at the-chamber.org <mailto:jmurray at the-chamber.org>.
--
-- Esther L., esther-L at alumni.virginia.edu
Speaking only for myself
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