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

Research"

Tuesday, Sept. 15, 3:30-5 p.m.

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

Kendle at Booth #706

Kendle experts will be available for on-site meetings and to discuss the Company's full suite of regulatory affairs capabilities at booth #706 in the exhibition hall.

Kendle offers extensive regulatory affairs experience, including delivery of all types of projects from global submissions to specialist consulting services. The Company provides expertise and advice at every stage of the drug development process, from early development to market and beyond. Kendle can ensure a product's development is conducted efficiently and in a timely manner, ensuring its smooth transition into the marketplace. The Company's Regulatory Affairs experts understand the commercial imperatives underlining decisions such as where to submit first, or which regulatory route to follow in a particular region, and work with biopharmaceutical companies worldwide to design an appropriate strategy for any product anywhere in the world.

Kendle offers customers global regulatory centers of expertise around the world to meet their needs. These integrated locations include Rockville, Maryland and Cincinnati, Ohio in the United States; Ely, England and Edinburgh, Scotland in Europe; Sydney and Melbourne, Australia in the Asia/Pacific region; and Mexico City, Mexico in Latin America.

About Kendle

Kendle International Inc. (Nasdaq: KNDL) is a leading global clinical research organization providing the full range of early- to late-stage clinical development services for the world's biopharmaceutical industry. Our focus is on innovative solutions that reduce cycle times for our customers
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SOURCE Kendle International Inc.
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