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International Journal of Pharmaceutics|August 5, 2014
Development of performance matrix for generic product equivalence of acyclovir topical creamsYellela S R Krishnaiah, Xiaoming Xu, Ziyaur Rahman, et al.Pharmacoepidemiology and Drug Safety|September 6, 2006
Risk minimization practices for pregnancy prevention: understanding risk, selecting toolsKathleen Uhl, Anne Trontell, Dianne KennedyDrug Safety|March 9, 2004
Pregnancy exposure registriesDianne L Kennedy, Kathleen Uhl, Sandra L KwederObstetrics and Gynecology|May 2, 2006
Antibiotic use in pregnancy and lactation: what is and is not known about teratogenic and toxic risksGerard G Nahum, Kathleen Uhl, Dianne L KennedyDrug Safety|September 21, 2002
Risk management strategies in the Physicians' Desk Reference product labels for pregnancy category X drugsKathleen Uhl, Dianne L Kennedy, Sandra L KwederJournal of Clinical Pharmacology|July 3, 2002
Advanced science education in the regulatory arena: the Center for Drug Evaluation and Research Experience at the Food and Drug AdministrationFunmilayo O Ajayi, Dale F Wilcox, Kathleen Uhl, et al.Expert Review of Clinical Pharmacology|November 26, 2011
Adverse effects in women: implications for drug development and regulatory policiesAmeeta Parekh, Emmanuel O Fadiran, Kathleen Uhl, et al.Women'S Health Issues : Official Publication of the Jacobs Institute of Women'S Health|March 11, 2009
Increasing participation of women in early phase clinical trials approved by the FDAEllen Pinnow, Pellavi Sharma, Ameeta Parekh, et al.Drug Discovery Today. Technologies|July 2, 2014
Drug eluting stents and the critical path initiative: Evolving paradigms for safety evaluationWendy R Sanhai, Norman Stockbridge, Robert P Fiorentino, et al.Current Medical Research and Opinion|January 6, 2006
Evaluation of the costs and outcomes from changes in risk factors in type 2 diabetes using the Cardiff stochastic simulation cost-utility model (DiabForecaster)Phil McEwan, John R Peters, Klas Bergenheim, et al.Pageof 4