[IEEE-bhpjobs] Learn all about the FDA and its regulations for Drugs, Biologics, and Devices

[Esther L.]

I enrolled in this last year.  I highly recommend it as a thorough 
introduction to the pharma/CRO industry. I did pass the RAC exam.  This 
course starts June 22nd. Information is also at 
https://www.ieeecommunities.org/encs?go=438559

I have found ASQ, NCRAF, and NCCSQA meetings useful for learning about 
the pharma/CRO industry.
Esther Lumsdon, RAC


-------- Original Message --------
Subject: 	NCRAF - RAC Training
Date: 	Tue, 15 Jun 2004 21:20:08 -0400
From: 	Lisa Olson <lolson at secassociates.com>



Dear NCRAF members and friends,
Once again, the North Carolina Regulatory Affairs Forum will be running
training for the Regulatory Affairs Certification Program.  Please see
the attached flyer.  This is available to NCRAF members, but you can
join and then attend!

Also - if you have a place in your organization to post this flyer on a
bulletin board or other location, please feel free to spread it around
(regulatory affairs department, QA, clinical, laboratories, cafeteria,
elevators).  And please also circulate at local professional meetings
that you may attend.

Note that the contact for this is Alexandra McCormick,
mccor025 at mc.duke.edu.

There may be an EU RAC course also, if there is interest.  If so, please
contact Clare Matti at camatti at nc.rr.com

Hope you can make it!  This is a wonderful opportunity to hear some
great lectures.

Lisa Olson
VP, Communications - NCRAF





-- 
-- Esther L. esther_L @ ieee.org, letter L, not a numeral.
Speaking only for myself

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