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Benefit-Risk Assessment in Pharmaceutical Research and Development

in drug development and commercialization. Helping to alleviate this knowledge gap, Benefit-Risk Assessment in Pharmaceutical Research and;

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BenefitRisk Appraisal of Medicines

tool for the assessment of benefits and risks for new medicines in development. This model utilises a multi-criteria decision analysis which;

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Design and Analysis of Animal Studies in Pharmaceutical Development

research and development. Demonstrates the correct way to interpret the results of animal studies in the risk assessment of biopharmaceutical;

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Design and Analysis of Animal Studies in Pharmaceutical Development

research and development. Demonstrates the correct way to interpret the results of animal studies in the risk assessment of biopharmaceutical;

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Health Risk Assessment Dermal and Inhalation Exposure and Absorption of Toxicants

in industrial, pesticide, and pharmaceutical development. The book will also benefit individuals in environmental, regulatory, and registration affairs;

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Pharmaceutical Quality by Design

agencies to ensure the development of a consistent and high-quality pharmaceutical product that safely provides the maximum therapeutic benefit to;

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Characterizing and Communicating Uncertainty in the Assessment of Benefits and Risks of Pharmaceutical Products

development process. Characterizing and Communicating Uncertainty in the Assessment of Benefits and Risks of Pharmaceutical Products summarizes the;

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Understanding the Benefits and Risks of Pharmaceuticals

All pharmaceutical products have inherent risks, and their use involves trade-offs between their therapeutic benefits and their risks;

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Revival

toxicologists, environmental chemists, pharmacologists, risk assessors, and managers working in industrial, pesticide, and pharmaceutical development.;

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Pharmaceutical Medicine and Translational Clinical Research

research into new medicines, also focusing on the need to understand the safety profile of medicine and the benefit-risk balance. Pharmacoeconomics;

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Understanding the Basics of QSAR for Applications in Pharmaceutical Sciences and Risk Assessment

Understanding the Basics of QSAR for Applications in Pharmaceutical Sciences and Risk Assessment describes the historical evolution;

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Risk Assessment Methods for Biological and Chemical Hazards in Food

, more specifically, new trends and approaches such as the development of risk rating methods, risk metrics, risk-benefit assessment studies and;

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Risk Assessment Methods for Biological and Chemical Hazards in Food

, more specifically, new trends and approaches such as the development of risk rating methods, risk metrics, risk-benefit assessment studies and;

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The Agile Approach to Adaptive Research

viewpoint that shows how adaptive research technology and methods benefit the drug industry. It gives readers a practical overview of drug;

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Quantitative Evaluation of Safety in Drug Development

development, covering Bayesian methods, effective safety graphics, and risk-benefit evaluation. Written by a team of experienced leaders, this book;

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Benefit-Risk Assessment Methods in Medical Product Development

Guides You on the Development and Implementation of B-R Evaluations Benefit-Risk Assessment Methods in Medical Product Development;

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How to Validate a Pharmaceutical Process

practitioners engaged in pharmaceutical process validation. Thoroughly referenced and based on the latest research and literature

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Mutagenic Impurities - Strategies for Identification and Control

development of effective control measures, including chapters on the purge tool for risk assessment. The book incorporates a discussion of N;

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Risk/Benefit Analysis for the Use and Approval of Thrombolytic, Antiarrhythmic, and Hypolipidemic Agents

The Symposium on New Drugs provides a forum for academic investigators, research and development personnel from the pharmaceutical industry;

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Nutraceuticals and Natural Product Pharmaceuticals

to benefit from this thorough resource. Connects research from the nutraceutical and pharmaceutical industries Promotes;

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The early benefit assessment in the context of the Act on the Reform of the Market for Medicinal Products (AMNOG)

healthcare system? To answer this question, this work first presents the theoretical foundations of the law, of the early benefit assessment and the;

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Pharmaceutical Microbiology

risk assessment tools and techniques. These key aspects are discussed through a series of dedicated chapters, with topics covering auditing;

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Hit and Lead Profiling

of filtering and risk assessment of potential new drug molecules before actual drug development, the two equally important aspects of pharmacological;

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Handbook of Recidivism Risk / Needs Assessment Tools

Provides comprehensive coverage on recidivism risk/needs assessment tools Correctional and healthcare professionals around the world;

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Process Systems Engineering for Pharmaceutical Manufacturing

, integrated flowsheets and applications for design, analysis, risk assessment, sensitivity analysis, optimization, design space identification and;

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Pharmaceutical Microbiological Quality Assurance and Control

pharmaceuticals microbiological QA/QC Presents the latest developments in both regulatory expectations and technical advancements Provides guidance on;

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Statistics in Drug Research

applications for each stage of pharmaceutical development to ensure the valid design, analysis, and assessment of drug products under investigation and;

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