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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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Chemical Engineering in the Pharmaceutical Industry

A guide to the development and manufacturing of pharmaceutical products written for professionals in the industry, revised second edition;

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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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Pharmaceutical Extrusion Technology

The first edition of Pharmaceutical Extrusion Technology, published in 2003, was deemed the seminal book on pharmaceutical extrusion. Now;

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Active Pharmaceutical Ingredients

To successfully bring an Active Pharmaceutical Ingredient (API) to market, many steps must be followed to ensure compliance with;

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Active Pharmaceutical Ingredients in Synthesis

. Active Pharmaceutical Ingredients in Synthesis: Catalytic Processes in Research and Development offers chapters covering: Catalysis and;

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Solid State Development of Pharmaceutical Molecules Salts, Cocrystals, and Polymorphsim

Solid State Development and Processing of Pharmaceutical Molecules A guide to the lastest industry principles for optimizing the production;

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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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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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Pharmaceutical Applications of Raman Spectroscopy

improvements in instrumentation, decreasing cost, and the availability of chemometrics to assist in the analysis of data. Pharmaceutical applications;

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Application of Nano/Microencapsulated Ingredients in Food Products

of global experts in the fields of nano and microencapsulation of food, nutraceutical and pharmaceutical ingredients, this title is of great value;

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An Introduction to Pharmaceutical Sciences

, regulation and marketing. The key theme of the book is pharmaceuticals - what every student of pharmaceutical sciences should know: from the active;

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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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Pharmaceutical Process Validation

The third edition of this text contains additional chapters which cover troubleshooting procedures, validation in contract manufacturing;

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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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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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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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Facility Validation

Often considered a necessary evil by the pharmaceutical industry, validation is still understood by many as unrestrained bureaucracy;

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Cactus Mucilage as Pharmaceutical Excipient

Excipients are additives, used to convert active pharmaceutical ingredients into pharmaceutical dosage form suitable for administration to;

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Particles and Nanoparticles in Pharmaceutical Products: Design, Manufacturing, Behavior and Performance

, pharmacological and toxicological characteristics - when they are a component of pharmaceutical products and formulations. The book discusses in detail;

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Pharmaceutical Master Validation Plan

. Pharmaceutical Master Validation Plan: The Ultimate Guide to FDA, GMP, and GLP Compliance will allow you to more easily achieve satisfactory inspections;

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Pharmaceutical Salts and Co-crystals

issues in the solid state science and particularly in the pharmaceutical world. In this context, multi-component crystalline materials like co;

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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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Tools For Chemical Product Design

range of sectors including gasoline additives and blends in the petroleum industry, active ingredients and excipients in the pharmaceutical;

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Retrosynthesis in the Manufacture of Generic Drugs

of some widely used drugs This book illustrates how the retrosynthetic tool is applied in the Pharmaceutical Industry. It considers and;

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Good Design Practices For Gmp Pharmaceutical Facilities

A convenient single-source reference for anyone involved in the planning, construction, validation, and maintenance of modern;

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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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