Pharmaceutical Industry Perspective on the Non-Clinical Evaluation of Novel Excipients: Results From an Industry Survey Conducted by the IQ Novel Excipient Working Group von Giffen, Paul S., Buckley, Lorrene A., Pinkstaff, Jason

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A cross-industry survey on photosafety evaluation of pharmaceuticals after implementation of ICH S10 von Bauer, Daniel, Buckley, Lorrene A., Delafoy, Laure, Ellinger-Ziegelbauer, Heidrun, Fellows, Mick D., Gerets, Helga H.J., Howe, Jonathan, Kaijser, Gerry, Nicolette, John, Pettersen, Betty A., Schimpf, Brian

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Pharmaceutical industry perspective on combination toxicity studies: Results from an intra-industry survey conducted by IQ DruSafe Leadership Group von Birkebak, Joanne, Buckley, Lorrene A., Dambach, Donna, Musvasva, Eunice, Price, Karen, Ralston, Sherry, Sacaan, Aida

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Challenges and strategies to facilitate formulation development of pediatric drug products: Safety qualification of excipients von Buckley, Lorrene A., Salunke, Smita, Thompson, Karen, Baer, Gerri, Fegley, Darren, Turner, Mark A.

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Estimation of acceptable daily intake values based on modeling and in vivo mutagenicity of NDSRIs of fluoxetine, duloxetine and atomoxetine von Jolly, Robert A., Cornwell, Paul D., Noteboom, Jessica, Sayyed, Fareed Bhasha, Thapa, Bishnu, Buckley, Lorrene A.

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Drug Development 101: A Primer von Buckley, Lorrene A., Bebenek, Ilona, Cornwell, Paul D., Hodowanec, Aimee, Jensen, Eric C., Murphy, Caitlin, Ghantous, Hanan N.

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The design of chronic toxicology studies of monoclonal antibodies: Implications for the reduction in use of non-human primates von Chapman, Kathryn L., Andrews, Laura, Bajramovic, Jeffrey J., Baldrick, Paul, Black, Lauren E., Bowman, Christopher J., Buckley, Lorrene A., Coney, Lee A., Couch, Jessica, Maggie Dempster, A., de Haan, Lolke, Jones, Keith, Pullen, Nick, de Boer, Anne Seitske, Sims, Jennifer, Ian Ragan, C.

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High dose selection in general toxicity studies for drug development: A pharmaceutical industry perspective von Buckley, Lorrene A., Dorato, Michael A.

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Considerations Regarding Nonhuman Primate Use in Safety Assessment of Biopharmaceuticals von Buckley, Lorrene A., Chapman, Kathryn, Burns-Naas, Leigh Ann, Todd, Marque D., Martin, Pauline L., Lansita, Janice A.

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The Toxicology Education Summit: building the future of toxicology through education von Barchowsky, Aaron, Buckley, Lorrene A, Carlson, Gary P, Fitsanakis, Vanessa A, Ford, Sue M, Genter, Mary Beth, Germolec, Dori R, Leavens, Teresa L, Lehman-McKeeman, Lois D, Safe, Stephen H, Sulentic, Courtney E W, Eidemiller, Betty J

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Nonclinical Assessment of Carcinogenic Risk and Tumor Growth Enhancement Potential of Prasugrel, a Platelet-Inhibiting Therapeutic Agent von Buckley, Lorrene A., Sanbuissho, Atsushi, Starling, James J., Knadler, Mary Pat, Iversen, Philip W., Jakubowski, Joseph A.

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Toxicology Testing in Drug Discovery and Development von Dorato, Michael A., Buckley, Lorrene A.

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Toxicology in the Drug Discovery and Development Process von Dorato, Michael A., Buckley, Lorrene A.

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Biologically-based models of dioxin pharmacokinetics von Buckley, Lorrene A.

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Carcinogenicity of 2',3'-dideoxycytidine in mice von RAO, G. N, COLLINS, B. J, GILES, H. D, HEATH, J. E, FOLEY, J. F, MAY, R. D, BUCKLEY, L. A

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Estimation of Human Starting Dose for Phase I Clinical Programs von Buckley, Lorrene A, Garhyan, Parag, Ponce, Rafael, Roberts, Stanley A

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Toxicology in the Drug Discovery and Development Process von Dorato, Michael A., Buckley, Lorrene A.

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Nonclinical Strategies for Investigating Potential Tumor Signals Detected in Clinical Trials von Buckley, Lorrene A., Silva-Lima, Beatriz, Tirmenstein, Mark A.

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Amidrazones. 4. Ylide syntheses von Smith, Richard F, Kinder, Laurie L, Walker, Donald G, Buckley, Lorrene A, Hammond, John M

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Amidrazones V. thermolysis of N 1-benzyl-substituted amidrazone ylides von Smith, Richard F., Craig, Allen S., Buckley, Lorrene A., Soelch, Richard R.

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