Recent Editorials/Articles

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.

	The Road to ePublishing Success Regulatory Affairs Focus, December 2006 Ken Ibbotson, Associate Director, Medical Writing, and Alex Yates, Senior Regulatory Consultant
	Global Development Regulatory Update: Australia Regulatory Affairs Focus, August 2006 Judith Bingham, BPharm, MHSc, GAICD, Director, Regulatory Development and Commercialization
	Access all areas: Global patient recruitment Good Clinical Practice Journal, June 2006 Janet Jones, PhD, Director, Global Patient Access and Retention
	Get with the Programme European Pharmaceutical Contractor, Summer 2006 Dr. Florian Eichmann, Dr. Dieter Komossa and Petra Ludwig of Kendle Global Late Phase
	FDA Postmarketing Commitment Studies Regulatory Affairs Focus, April 2006 Jean Siebenaler, MD, Global Medical Director, Late Phase
	Late Phase Studies Get Real The CenterWatch Monthly, April 2006 Cynthia Verst-Brasch, PharmD, Vice President, Late Phase Jean Siebenaler, MD, Global Medical Director, Late Phase
	Best of Both Worlds International Clinical Trials, Spring 2006 Jean Siebenaler, MD, Global Medical Director, Late Phase
	Elements of Risk Assessment and Risk Minimization Regulatory Affairs Focus, March 2006 Kenneth Hintze, PhD, Senior Director, Global Safety and Pharmacovigilance Melanie Bruno, PhD, MBA, Vice President Regulatory Affairs and Quality
	Leveraging Latin assets in clinical trials Good Clinical Practice Journal, March 2006 Dennis P. Hurley, DrSc, Vice President Global Clinical Development - Latin America
	A Practical Guide: Analysis of Variance and Covariance: A Gentle Introduction Pharmaceutical Physician, March 2006 Michael Bramley, Senior Biostatistician Richann Watson, Biostatistician
	Diabetes: Vive la différence Good Clinical Practice Journal, February 2006 Jean Siebenaler, MD, Global Medical Director, Late Phase
	Strategic Regulatory Planning: Setting the Stage for Success Regulatory Affairs Focus, February 2006 William Sietsema, PhD, Vice President, Clinical and Regulatory Strategic Planning Melanie Bruno, PhD, MBA, Vice President Regulatory Affairs and Quality
	A Practical Guide: Increasing Statistical Comprehension with Two Useful Methods: Confidence Intervals and the t-Test Procedure Pharmaceutical Physician, January 2006 Dennis Hurley, Vice President, Global Clinical Development - Latin America David Sotres-Ramos, Chief Statistical Officer for Latin America Claudia Lara-Perez-Soto, Manager of Biostatistics Rebeca Ponce-de-Leon, Manager, Clinical Quality Assurance and Medical Writing

Files require Adobe Acrobat Reader