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Statistical Design and Analysis in Pharmaceutical Science: Validation, Process Controls, and Stability

Offers a comprehensive, unified presentation of statistical designs and methods of analysis for all stages of pharmaceutical development;

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Statistical Design and Analysis in Pharmaceutical Science

Offers a comprehensive, unified presentation of statistical designs and methods of analysis for all stages of pharmaceutical development;

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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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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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Statistical Design and Analysis of Stability Studies

, Statistical Design and Analysis of Stability Studies presents the principles and methodologies in the design and analysis of stability studies;

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Statistical Design and Analysis of Stability Studies

, Statistical Design and Analysis of Stability Studies presents the principles and methodologies in the design and analysis of stability studies;

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Endtoend Data Analytics for Product Development

and the design of experiments (DoE) whilst covering the basic statistical concepts useful to an understanding of DoE. The text supports;

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Validation of Pharmaceutical Processes

edition of Validation of Pharmaceutical Processes examines and blueprints every step of the validation process needed to remain compliant and;

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How to Validate a Pharmaceutical Process

process validation program. The latest volume in the Expertise in Pharmaceutical Process Technology Series, this book illustrates the methods and;

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Innovative Statistics in Regulatory Science

). This book provides key statistical concepts, innovative designs, and analysis methods that are useful in regulatory science. Also included are;

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Innovative Statistics in Regulatory Science

selection and complex innovative design such as adaptive trial design) in the pharmaceutical development and regulatory approval process;

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Pharmaceutical Experimental Design

This useful reference describes the statistical planning and design of pharmaceutical experiments, covering all stages in the development;

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Pharmaceutical Experimental Design

This useful reference describes the statistical planning and design of pharmaceutical experiments, covering all stages in the development;

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Pharmaceutical Manufacturing Handbook

. In addition, the book discusses quality assurance and validation, drug stability, and contamination control, all key aspects of pharmaceutical;

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How to Sell Validatable Equipment to Pharmaceutical Manufacturers

equipment design and construction, documentation requirements, avoiding validation pitfalls, and the types of services the supplier should provide;

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Pharmaceutical Engineering Change Control

computer validation, customization of the change process to each project's needs, and case histories and anecdotes illustrate key points and;

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Pharmaceutical Engineering Change Control

computer validation, customization of the change process to each project's needs, and case histories and anecdotes illustrate key points and;

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Solid Oral Dose Process Validation, Volume Two

Process Validation, Lifecycle Approach: Application, Volume Two and the companion Volume One, Solid Dose Process Validation, The Basics, also;

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Automation Applications in Bio-pharmaceuticals

professional, this book outlines the unique design and application issues for the bio-pharmaceutical industry. For those already familiar with this;

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Pharmaceutical Dosage Forms - Parenteral Medications: Volume 3: Regulations, Validation and the Future

development. As such, it is recommended for scientists and engineers in the pharmaceutical industry and academia, and will also serve as an excellent;

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Solid Oral Dose Process Validation

approach solid dose manufacturing process validation for regulatory compliance. Solid Dose Process Validation: The Basics, Volume One and companion;

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Intro To Statistical Analysi Of Lab Data

of assay design and validation as well as fit for purpose procedures including real world examples * Includes a rigorous review of statistical;

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Method Validation in Pharmaceutical Analysis

Design (QbD) and lifecycle concepts in pharmaceutical manufacturing. As in the first edition, the fundamental requirements for analytical method;

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Solid-State Properties of Pharmaceutical Materials

, and pharmaceutical product development * Introduces appropriate manufacturing and control procedures using Quality by Design, and other;

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Dose Finding in Drug Development

analysis of clinical trials. Many of the discussions are based on applications of statistical methods in the design and analysis of dose response;

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Statistical and Multivariate Analysis in Material Science

give the readers basic knowledge on how statistical reasoning is exploitable in this field, improving their knowledge of statistical tools and;

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Facility Validation

, commissioning, and validation activities can be integrated and streamlined to accelerate a pharmaceutical manufacturing plant start-up effort, and;

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