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Kendle Experts to Share Insights at the Regulatory Affairs Professionals Society Annual Conference and Exhibition
Date:9/11/2009

CINCINNATI, Sept. 11 /PRNewswire-FirstCall/ -- Kendle (Nasdaq: KNDL), a leading, global full-service clinical research organization, today announced that its regulatory affairs experts will share their insights on key industry topics at the Regulatory Affairs Professionals Society (RAPS) Annual Conference and Exhibition to be held Sept. 13-16 at the Pennsylvania Convention Center in Philadelphia. Demonstrating its leadership position in providing regulatory guidance to its global pharmaceutical customers across the Phase I through IV clinical development process, Kendle has been selected to lead five sessions at the conference.

(Logo: http://www.newscom.com/cgi-bin/prnh/20080923/CLTU095LOGO)

Kendle's presentations include:

"New Pregnancy and Lactation Labeling Rule Revisions"

Monday, Sept. 14, 11 a.m.-Noon

Lisa Jenkins, PhD, Group Leader, Regulatory Consulting and Submissions

"Drug/Biologic Preapproval Inspection (PAI) - A Survival Guide"

Monday, Sept. 14, 1:30-3 p.m.

Hari Nagaradona, PhD, Associate Director, Regulatory Consulting and Submissions

"Adaptive Clinical Trial Designs That Get Results"

Monday, Sept. 14, 1:30-3 p.m.

Lisa Jenkins, PhD, Group Leader, Regulatory Consulting and Submissions

"The Expanding Role of Regulatory Advice: Guidance meets Business Development Professional " - Panel Discussion

Monday, Sept. 14, 1:30-3 p.m.

William Sietsema, PhD, Vice President, U.S. Regulatory Consulting and Submissions

"Ethical Standards in Clinical
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SOURCE Kendle International Inc.
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