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Development and Validation of Chromatographic Methods for Simultaneous Quantification of Drugs in Bulk and in Their Formulations

of moxifloxacin hydrochloride and dexamethasone sodium phosphate in combined pharmaceutical dosage form. 3. Development and validation of a RP-HPLC method;

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HPLC Method Development and Validation in Pharmaceutical Analysis

This handbook is concerned with new chromatographic method development and validation using novel systematic approaches for pharmaceutical;

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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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Handbook of Analytical Validation

regulatory requirements on the validation of new or modified analytical methods. Shedding light on method validation from a practical standpoint, the;

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Practical Approaches to Method Validation and Essential Instrument Qualification

calibration of instruments and validation of analytical methods. Advance Technologies in Instrumentation, Qualification, Performance, Verification and;

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Handbook of Pharmaceutical Analysis by HPLC

technique in pharmaceutical analysis and is predominantly used in the pharmaceutical industry. Written by selected experts in their respective;

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Validation of Pharmaceutical Processes

of equipment; analytical methods, calibration and certification. As the industry's leading source for validation of sterile pharmaceutical processes;

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Specification of Drug Substances and Products: Development and Validation of Analytical Methods

Specification of Drug Substances and Products: Development and Validation of Analytical Methods, Second Edition, presents a comprehensive;

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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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Principles and Practices of Method Validation

the validation of new methods for pesticide residue analysis in foodstuffs and water but the principles can be applied to other similar fields;

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Sample Preparation of Pharmaceutical Dosage Forms

typically used with pharmaceutical dosage forms. * Part Three discusses sample preparation method development for different types;

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Finite Element Analysis - Method, Verification and Validation, Second Edition

and updated second edition of Finite Element Analysis: Method, Verification, and Validation offers a comprehensive review of the theoretical;

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HPLC Method Development for Pharmaceuticals

product. HPLC Method Development for Pharmaceuticals provides an extensive overview of modern HPLC method development that addresses these unique;

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Handbook of Analytical Quality by Design

Handbook of Analytical Quality by Design addresses the steps involved in analytical method development and validation in an effort to;

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Experimentation, Validation, and Uncertainty Analysis for Engineers

of experimentation, validation, and uncertainty analysis Emphasizes the use of the Monte Carlo Method in performing uncertainty analysis Includes complete;

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Solid Oral Dose Process Validation, Volume Two

pharmaceutical preparations, it is essential information for pharmaceutical professionals who use the process validation lifecycle approach. This set;

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Pharmaceutical Analysis for Small Molecules

Compendial Approval Process (public standards) Common methods in pharmaceutical analysis (typically compendial) Common Calculations for assays and;

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How to Sell Validatable Equipment to Pharmaceutical Manufacturers

of discussion include: o Validation and GMP issues o Why validation is so important to pharmaceutical manufacturers o The role of equipment;

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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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Pharmaceutical and Medical Applications of Near-Infrared Spectroscopy

, and film coating of beads or granules Pharmaceutical assays, including qualitative analysis, quantitative analysis, determination;

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Pharmaceutical and Medical Applications of Near-Infrared Spectroscopy

, and film coating of beads or granules Pharmaceutical assays, including qualitative analysis, quantitative analysis, determination;

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Automation and Validation of Information in Pharmaceutical Processing

pharmaceutical information automation from industry and system automation professionals-demonstrating how to fulfill computer system validation;

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Validation of Active Pharmaceutical Ingredients

Much has happened in the area of bulk pharmaceutical good manufacturing practice (GMP) and validation since the first publication;

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Spectrophotometric determination of diaveridine and two sulfa drugs

be achieved by the use of spectrophotometery for quantitative analysis of pharmaceutical compounds. Several spectrophotometric methods are;

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Target Discovery and Validation

pharmaceutical chemists, Target Discovery and Validation explores the current methods for the identification and validation of drug targets in one;

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HPLC for Pharmaceutical Scientists

and method validation. Practical and pragmatic approaches and actual examples of effective development of selective and rugged HPLC methods;

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Solid Oral Dose Process Validation

majority of the pharmaceutical preparations, it is essential information for pharmaceutical professionals who use the process validation lifecycle;

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