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Kendle Experts to Present at the Drug Information Association 44th Annual Meeting
Date:6/19/2008

CINCINNATI, June 19 /PRNewswire-FirstCall/ -- Kendle (Nasdaq: KNDL), a leading global full-service clinical research organization (CRO), today announced that several of its experts will present at the upcoming Drug Information Association (DIA) 44th Annual Meeting. The meeting is scheduled for June 22-26, 2008, at the Boston Convention and Exhibition Center in Boston, Mass. Kendle's experts will speak on key topics in the clinical development industry, including EDC, biomarkers, regulatory affairs, adaptive clinical trial design, professional development and patient access and retention.

(Logo: http://www.newscom.com/cgi-bin/prnh/20030429/KNDLLOGO )

In addition to attending presentations by Kendle speakers, attendees at the DIA Annual Meeting may visit Kendle experts at two booths in the exhibit hall. Booth 1804 will focus on the company's global Phase I-IV service offerings and will preview its recently expanded Early Phase capabilities following the June 2 acquisition of DecisionLine Clinical Research Corporation, an early phase CRO specializing in the conduct of Phase I studies involving the measurement of pharmacodynamic effects of central nervous system (CNS) drugs. Booth 456 will focus on career opportunities at Kendle.

Kendle speakers include:

June 23

EDC: Faster Horse or Model T?

Sylva Collins, PhD, Vice President, Global Biometrics

10:30 a.m. - 12 p.m.

June 24

Biomarkers and Surrogate Endpoints: Definitions, Background, and

Validation

Lisa Jenkins, PhD, Regulatory Group Leader

8 - 9:30 a.m.

General Process and Best Practices for EOP2 and Pre-
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SOURCE Kendle International Inc.
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