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The top documents tagged [dose groups]
September 16, 2005 Statistical Methods for Testing Carcinogenic Potential of New Drugs in Animal Carcinogenicity Studies Hojin Moon, Ph.D. HMoonnctr.fda.gov
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Issues and Experience in Analyzing Transgenic Mouse Carcinogenicity Studies: An Industry Perspective Ronald Menton Wyeth Research 2005 FDA/Industry Statistics
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Biomarkers and Surrogate Endpoints in Drug Development Technical and Regulatory Considerations Biomarkers and Surrogate Endpoints in Drug Development Technical
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Real-Time Quantitative Reverse Transcription Polymerase Chain Reaction (qRT-PCR) Analysis Jelena Brkic BIOL5081
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Animal toxicology studies
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Characterization of inflammation and immune cell modulation induced by low- dose LPS administration to healthy volunteers M.R. Dillingh 1, E.P. van Poelgeest
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American Conference on Pharmacometics –San Diego, CA; April 3-6 2011 Population PK modeling incorporating enzyme induction mechanism to guide the design
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John C. O’Connor DuPont Haskell Laboratory for Health and Environmental Sciences The 15-Day Intact Adult Male Assay As An Alternative Tier I Screening
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Human endotoxin model – introduction
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Organized and Effective Interpretation of Clinical Laboratory Data: Graphs Make a Difference Robert Gordon Biostatistics and Medical Safety Johnson & Johnson
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Drug Supply Management for Adaptive Trials Micheline Marshall (Pfizer) Nancy Burnham (GlaxoSmithKline) NitinPatel (Cytel Inc) March 12, 2010 On behalf
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111 Department of Statistics TEXAS A&M UNIVERSITY STAT 211 Instructor: Keith Hatfield
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