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Kendle Experts to Address Key Industry Issues at Drug Information Association 47th Annual Meeting
Date:6/16/2011

CINCINNATI, June 16, 2011 /PRNewswire/ -- Kendle (Nasdaq: KNDL), a leading, global full-service clinical research organization, today announced several of its senior clinical development experts will present on important industry issues at the Drug Information Association (DIA) 47th Annual Meeting, June 19-23, 2011, in Chicago. Kendle experts will address key topics, including the benefits of hybrid monitoring; finding an economic balance between cost and reimbursement; and strategic development planning for clinical trials programs. Company executives will be available throughout the conference at booth #1343 for on-site meetings and to discuss why partnering with Kendle is an important step toward clinical development project success.

The 2011 DIA Annual Meeting bills itself as the "largest global, multidisciplinary gathering of biopharmaceutical professionals whose agenda is clear: to find immediate solutions to the most pressing needs of our industry for today and tomorrow." With the cost of drug development today estimated at well over $1 billion, the biopharmaceutical industry is under immense and growing pressure to drive efficiencies into the clinical development process and control costs. Partnering with global CROs, such as Kendle, that offer strong geographic, therapeutic and functional expertise across Phase I through IV is an important part of the solution. Independent research by the Tufts Center for the Study of Drug Development indicates clinical trials conducted by CROs are completed an average of 30 percent more quickly than those conducted in-house, resulting in an average time savings of four to five months and translating to $120 million to $150 million in increased revenue potential.

Kendle Speakers at DIA:

Tuesday, June 21, 10-11:30 a.m., Session 213, Room W181a
Symposium: Monitoring and Source Verification: New A
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SOURCE Kendle International Inc.
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