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Equipment Qualification in the Pharmaceutical Industry

Equipment Qualification in the Pharmaceutical Industry provides guidance and basic information for the preparation of a quality;

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Pharmaceutical Equipment Validation

validation. The author provides a thorough understanding of how to prepare, test, and complete equipment qualification protocols. He also explains;

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Pharmazeutische Produkte und Verfahren

pharmaceutical production plants, production processes, equipment and machinery, as well as the accompanying qualification and validation measures;

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Pharmaceutical Dissolution Testing

, this reference provides reader-friendly chapters on currently utilized equipment, equipment qualification, consideration of the;

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Validation and Qualification in Analytical Laboratories

validation strategy for routine, non-routine, and standard analytical methods, covering the entire equipment, hardware, and software qualification;

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Calibration in the Pharmaceutical Laboratory

the use of equipment in their industry. The regulation of test and measuring equipment changes continually as new regulations are introduced;

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Filtration and Purification in the Biopharmaceutical Industry, Third Edition

of bioprocessing including the current methods, processes, technologies and equipment. It also covers industry standards and regulatory requirements for;

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Commissioning, Qualification and Validation

Commissioning, Qualification and Validation (CQV) are requirements of modern facilities within the Life Science industry. Be it a Medical;

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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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Piping and Pipelines Assessment Guide

of equipment is the bread and butter of any process plant. Used in the petrochemical industry, pharmaceutical industry, food processing industry, paper;

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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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Freeze Drying of Pharmaceutical Products

Freeze Drying of Pharmaceutical Products provides an overview of the most recent and cutting-edge developments and technologies in the;

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Pharmaceutical Analysis for Small Molecules

A comprehensive introduction for scientists engaged in new drug development, analysis, and approvals Each year the pharmaceutical;

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Handbook of Pharmaceutical Wet Granulation

Handbook of Pharmaceutical Wet Granulation: Theory and Practice in a Quality by Design Paradigm offers a single and comprehensive reference;

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GMP in Pharmaceutical Industry

This handbook has been written for the students of pharmacy and pharmaceutical industry. It gives pocket guide of good manufacturing;

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Canadian Heavy Equipment Technician

This handbook is an essential tool for any Heavy Equipment technician preparing to write their Certificate of Qualification exam. The book;

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Operational Excellence in the Pharmaceutical Industry

Operational Excellence in the Pharmaceutical Industry is een boek van Editio Cantor;

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Pharmaceutical Master Validation Plan

required to develop and execute a successful Master Validation Plan based on FDA guidelines for the pharmaceutical industry, and allows the;

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Modern Pharmaceutical Industry

Modern Pharmaceutical Industry comprehensively explains the broad range of divisions in the complex pharmaceutical industry. Experts who;

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Product Design And Engineering

. Recommended reading for process, pharma and chemical engineers, chemists in industry, and those working in the pharmaceutical, food, cosmetics, dyes;

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The Path from Biomarker Discovery to Regulatory Qualification

The Path from Biomarker Discovery to Regulatory Qualification is a unique guide that focuses on biomarker qualification, its;

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Pharmaceutical Industry Practices on Genotoxic Impurities

management by presenting rationales, strategies, methods, interpretations, practices, and case studies from the pharmaceutical industry. Featuring;

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Devalued and Distrusted

An expert's view on solving the challenges confronting today's pharmaceutical industry Author John LaMattina, a thirty-year veteran of the;

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The Indian Pharmaceutical Industry

This study analyzes the impact of the revision of the Indian Patent Act (2005) on the Indian pharmaceutical industry, which has been;

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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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Method Validation in Pharmaceutical Analysis

Performance Qualification, and Continued Method Performance Verification. Case studies and examples from the pharmaceutical industry illustrate the;

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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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