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

explores the most recent trends in the digitization and automation of the pharmaceutical production processes that reflect the need for consistent;

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Advanced Aseptic Processing Technology

, engineering, development, facility and equipment design, component and equipment suppliers, automation, and robotics.;

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Automation Applications in Bio-pharmaceuticals

This book is a guide for engineers and designers new to the field of bio-pharmaceutical process control. For the experienced automation;

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Endotoxins

, automation, depyrogenation. Completely revised and expanded, this Third Edition contains the knowledge necessary to apply endotoxin testing in the;

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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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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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Aseptic Pharmaceutical Manufacturing II

Asceptic Pharmaceutical Manufacturing II explores the sophisticated technology, developments, and applications that allow aseptic;

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Aseptic Pharmaceutical Manufacturing II

Asceptic Pharmaceutical Manufacturing II explores the sophisticated technology, developments, and applications that allow aseptic;

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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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Practical Pharmaceutical Laboratory Automation

successfully automate or interface equipment in the lab. A step-by-step, how-to reference and guide, Practical Pharmaceutical Laboratory Automation;

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Practical Pharmaceutical Laboratory Automation

successfully automate or interface equipment in the lab. A step-by-step, how-to reference and guide, Practical Pharmaceutical Laboratory Automation;

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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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New Developments in Clinical Instrumentation

This book has information regarding the new developments in clinical instrumentation, focusing on fluorometers and densitometers;

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Cleaning Validation Manual

, and validation of bio pharmaceuticals on a pilot scale, leading to scale-up production. With over 20 easy-to-use template protocols for;

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Cleaning Validation Manual

, and validation of bio pharmaceuticals on a pilot scale, leading to scale-up production. With over 20 easy-to-use template protocols for;

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Validating Corporate Computer Systems

practical information and advice on good IT practice and validation principles. Written by experts, it includes case studies on EDMSs, EAM systems;

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Validating Corporate Computer Systems

practical information and advice on good IT practice and validation principles. Written by experts, it includes case studies on EDMSs, EAM systems;

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Pharmaceutical Pelletization Technology

This book serves as a formulation and processing guide during the development of pelletized dosage forms. It provides the pharmaceutical;

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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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Pharmaceutical Process Scale-Up

The third edition of Pharmaceutical Process Scale-Up deals with the theory and practice of scale-up in the pharmaceutical industry. This;

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Pharmaceutical and Medical Devices Manufacturing Computer Systems Validation

information to assist in the computer validation to production systems, while highlighting and efficiently integrating worldwide regulation into the;

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Pharmaceutical and Medical Devices Manufacturing Computer Systems Validation

information to assist in the computer validation to production systems, while highlighting and efficiently integrating worldwide regulation into the;

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Advanced Hybrid Information Processing

sections as follows: Industrial application of multi-modal information processing; Industrialized big data processing; Industrial automation and;

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Advanced Hybrid Information Processing

sections as follows: Industrial application of multi-modal information processing; Industrialized big data processing; Industrial automation and;

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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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