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Encyclopedia of Biopharmaceutical Statistics 2nd Ed (Malestrom)
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Encyclopedia of Biopharmaceutical Statistics 2nd Ed (Malestrom) (Size: 61.96 MB) (Files: 195)
Validity of LOCF.pdf
Z-Score.pdf
Validation of Quantitative and Qualitative Assays.pdf
USP Tests.pdf
Vaccine Clinical Trials.pdf
Two-Stage Design- Phase II Cancer Clinical Trials.pdf
Toxicological Studies.pdf
Trend Estimation.pdf
Titration Design.pdf
Testing for Qualitative Interaction.pdf
Therapeutic Equivalence.pdf
Survival Analysis.pdf
Subgroup Analysis.pdf
Subject-Treatment Interaction.pdf
Stuart-Maxwell Test.pdf
Structural Equation Model.pdf
Statistical Tests for Biomarker Development with Applications to Genetics Data.pdf
Statistical Process Control.pdf
Statistical Significance.pdf
Statistical Principles for Clinical Trials.pdf
Stability Matrix Designs.pdf
SROC Curve.pdf
Stability Analysis for Frozen Drug Products.pdf
Spatio-Temporal Modeling.pdf
Specifications.pdf
Slope Approach for Assessment of Dose Proportionality-Linearity Under a Crossover Design.pdf
Sequential Estimation for the Additive Hazards Rate Model with Staggered Entry.pdf
Screening Design.pdf
Selection of Control in Clinical Trials.pdf
Sample Size Re-estimation Based on Observed Treatment Difference.pdf
Sample Size Determination.pdf
Sample Size Calculation for Survival Data.pdf
ROC Curve.pdf
Sample Size Calculation Based on Nonparametric Statistics.pdf
Robust Analysis for Crossover Design.pdf
Response Surface Methodology.pdf
Risk Ratio Analysis.pdf
Reproductive-Developmental Studies.pdf
Reliability.pdf
Reproducibility Probability in Clinical Research.pdf
Release Targets.pdf
Randomization.pdf
Rank Regression in Stability Analysis.pdf
QT Analysis.pdf
Proportional Hazards Regression Model.pdf
Protocol Development.pdf
Profile Analysis.pdf
Proportion of Treatment Effect.pdf
Principal Component Analysis.pdf
Process Validation.pdf
Power.pdf
Prediction Trees.pdf
Postmarketing Adverse Drug Event Signaling.pdf
Postmarketing Surveillance.pdf
Population Bioequivalence.pdf
Population PK-PD Analysis.pdf
Phase I Cancer Clinical Trials.pdf
Placebo Effect.pdf
Pharmacodynamics with No Covariates.pdf
Pharmacoeconomics.pdf
Pharmacodynamic Issues.pdf
Pharmacodynamics with Covariates.pdf
Percentile Charts on Correlated Measures.pdf
Parallel Design.pdf
Patient Compliance.pdf
P-Values.pdf
Outlier Detection in Clinical Research.pdf
P-Values, Evidence and Multiplicity Considerations for Controlled Clinical Trials.pdf
Ordered Multiple Class Receiver Operating Characteristic (ROC) Analysis.pdf
Odds Ratio.pdf
Onset of Action.pdf
Noninferiority Analysis in Active Controlled Clinical Trials.pdf
Multicollinearity.pdf
Multinational Clinical Trial.pdf
Modified Large Sample Method.pdf
Multicenter Trials.pdf
Mixed Effects Models.pdf
Missing Values in Repeated Measurement Designs.pdf
Minimum Effective Dose.pdf
Microarray Gene Expression.pdf
Minimization Procedure.pdf
Meta-Analysis of Therapeutic Trials.pdf
MedDRA and Its Impact on Pharmaceutical Development.pdf
Medical Devices.pdf
McNemar's Test.pdf
Measuring Agreement.pdf
Maximum Tolerable Dose for Cancer Chemotherapy.pdf
Logistic Regression in Three-Point Designs.pdf
Logistic Regression.pdf
Lilly Reference Ranges.pdf
Local Influence Analysis.pdf
Laboratory Analyses.pdf
Latent Class Analysis.pdf
Kullback-Leibler Divergence for Evaluating Equivalence.pdf
Coefficients in Medical Research.pdf
Kaplan-Meier Estimator.pdf
Investigating Quality-of-Life in Clinical Trials.pdf
International Conference on Harmonization (ICH).pdf
Interactive Voice Randomization System (IVRS).pdf
Interim Analysis.pdf
Intention-to-Treat Analyses (ITT).pdf
Instrument Development and Validation.pdf
Integrated Summary Report.pdf
Individual Bioequivalence.pdf
In Vitro Micronucleus Test.pdf
In Vitro Bioequivalence Testing.pdf
In Vitro Dissolution Profile Comparison.pdf
Imputation with Item Nonrespondents.pdf
Imputation in Clinical Research.pdf
Hypotheses and False Positive Rate in Active Control Non-Inferiority Trials.pdf
Group Sequential Tests and Variance Heterogeneity in Clinical Trials.pdf
Good Statistics Practice.pdf
Group Sequential Methods.pdf
Good Programming Practice.pdf
Global Database and System.pdf
Good Clinical Practice.pdf
Genetic Linkage and Linkage Disequilibrium Analysis.pdf
Generalized Estimating Equations (GEE) Method- Sample Size Estimation.pdf
Generalized Estimating Equation.pdf
Generalizability Probability in Clinical Research.pdf
False Discovery Rate (FDR).pdf
Food and Drug Administration.pdf
Factorial Designs.pdf
Failure-Time Model.pdf
Factor Analysis.pdf
Exploratory Factor Analysis.pdf
Extra Variation Models.pdf
Ethnic Factors.pdf
Expiration Dating Period.pdf
Enrichment Design.pdf
Equivalence Trials.pdf
Ecologic Inference.pdf
ED50-ED90.pdf
Dropout.pdf
Drug Development.pdf
Dose Response Study Design.pdf
Dose Proportionality.pdf
Dose Response Analysis in Clinical Trials.pdf
Diagnostic Imaging.pdf
Data Mining and Biopharmaceutical Research.pdf
Data Monitoring Committees (DMC).pdf
Crossover Design.pdf
Cutoff Designs.pdf
Cost-Effectiveness Analysis.pdf
Contract Research Organization (CRO).pdf
Correlated Probit Model.pdf
Content Uniformity.pdf
Confidence Interval and Hypothesis Testing.pdf
Confounding and Interaction.pdf
Comparing Variabilities in Clinical Research.pdf
Combination Drug Clinical Trial.pdf
Cluster Trials.pdf
Clustered Study Designs- Power Analysis.pdf
Clinical Trials.pdf
Clinical Trial Simulations for Later Development Phases.pdf
Clinical Trial Simulation.pdf
Clinical Trial Simulations for Earlier Development Phases.pdf
Clinical Trial Process.pdf
Clinical Endpoint.pdf
Clinical Pharmacology.pdf
Clinical Data Management.pdf
Case-Control Studies, Inference in.pdf
Center Weighting in Multicenter Trials.pdf
Carry-Forward Analysis.pdf
Cancer Trials.pdf
Carcinogenicity Studies of Pharmaceuticals.pdf
Calibration.pdf
Bracketing Design.pdf
Bridging Studies.pdf
Blinding.pdf
Bootstrap, The.pdf
Biologics.pdf
Biopharmaceutics.pdf
Bioinformatics.pdf
Bioassay.pdf
Bioavailability and Bioequivalence.pdf
Bayesian Two-Stage Design for Phase II Clinical Trials.pdf
Bayesian Statistics.pdf
Bayesian Methods in Meta-Analysis.pdf
Assay Validation.pdf
Assay Development.pdf
Analysis of Variance.pdf
ANCOVA Approach for Premarketing Shelf Life Determination with Multiple Factors .pdf
Analysis of Repeated Measures Data with Missing Values- An Overview of Methods .pdf
Analysis of Heritability.pdf
Analysis of Clustered Binary Data.pdf
Analysis of 2 K Tables .pdf
Ames Test.pdf
Alpha Spending Function.pdf
Adverse Event Reporting.pdf
Adjustment for Covariates.pdf
Adaptive Dose-Finding Based on Efficacy-Toxicity Trade-Offs .pdf
Adaptive Designs.pdf
Active Control Trials.pdf
Acceptance Sampling.pdf
Torrent description
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Shein-Chung Chow, “Encyclopedia of Biopharmaceutical Statistics”
Informa HealthCare | 2003-06-04 | ISBN: 0824742613 | 1000 pages | PDF
Millennium Pharmaceuticals, Cambridge, MA. Resource offers more than 3,300 lists expanded to reflect amendments to regulatory requirements and recently developed statistical methods impacting the drug review/approval process and biopharmaceutical research and development. Offers more than 3,000 equations, tables, and figures.
