Following are recent articles providing perspective from Kendle subject matter experts on various clinical development topics, therapeutic areas or current industry trends. New material is added frequently, so check back again soon to view the latest updates.
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News Focus: EU Paediatric Legislation, "What's the verdict, so far?"
Good Clinical Practice Journal, December 2004
Alan Davies, MD, MRCP, European Medical Director |
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PACKAGING Issues: Moving Drug Products From Prescription to Over-the-Counter Status
Regulatory Affairs Focus, November 2004
Salvatore J. Pinella, Senior Consultant, AAC Consulting Group, Inc., a subsidiary of Kendle. Melanie A. Bruno, PhD, MBA, Vice President, Regulatory Affairs |
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Era of Efficiency? Provider Selection and the RFP Process
PharmaVOICE, November 2004
Simon Higginbotham, Vice President and Chief Marketing Officer |
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Trials and Tribulations: Conducting clinical trials for combination products will lead manufacturers into a whole new world
MX, September/October 2004
Peter Adams, PhD, Senior Regulatory Affairs Consultant
Alan Davies, MD, MRCP, European Medical Director
Eduardo March, Senior Consultant
William K. Sietsema, PhD, Vice President, Clinical Development |
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Opportunities and Challenges of Pan European Post-Marketing Surveillance Programmes
European Biopharmaceutical Review, Autumn 2004
Wendy M. Shaw, PhD, Associate Director, Late Phase |
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Trials Around the World
PharmaVOICE, September 2004
Alan Davies, MD, MRCP, European Medical Director |
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The State of CME At the End of the Tunnel
PharmaVOICE, July 2004
Kathy Farwick, Director, Scientific Events, Education and Publications |
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Managing Outcomes
PharmaVOICE, July 2004
Andrea Spannheimer, Director, Health Economics and Outcomes Research |
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