Pharmaceutical Water

Pharmaceutical Water
Author: William V. Collentro
Publsiher: CRC Press
Total Pages: 478
Release: 2016-04-19
ISBN 10: 142007783X
ISBN 13: 9781420077834
Language: EN, FR, DE, ES & NL

Pharmaceutical Water Book Review:

A major new work on all aspects of water, the most used raw material ingredient in the pharmaceutical and biotechnology industries-used as an excipient in pharmaceutical formulations, as a cleaning agent, and as a separately packaged product diluent.Drawing on the author's extensive field experience with more than 400 pharmaceutical and related wat

Pharmaceutical Water Systems

Pharmaceutical Water Systems
Author: Theodore H. Meltzer
Publsiher: Tall Oaks Pub
Total Pages: 871
Release: 1996-01-01
ISBN 10: 9780927188067
ISBN 13: 0927188066
Language: EN, FR, DE, ES & NL

Pharmaceutical Water Systems Book Review:

Fate of Pharmaceuticals in the Environment and in Water Treatment Systems

Fate of Pharmaceuticals in the Environment and in Water Treatment Systems
Author: Diana S. Aga
Publsiher: CRC Press
Total Pages: 408
Release: 2007-12-26
ISBN 10: 9781420052336
ISBN 13: 1420052330
Language: EN, FR, DE, ES & NL

Fate of Pharmaceuticals in the Environment and in Water Treatment Systems Book Review:

The detection of pharmaceutical residues remained elusive until instruments such as liquid chromatography and mass spectrometry became commonplace in environmental laboratories. The documentation of the occurrence of pharmaceutical residues and endocrine disrupting chemicals in water resources has raused questions about their long-term effects in the ecosystem and their potential effects on human health. Fate of Pharmaceuticals in the Environment and in Water Treatment Systems covers critical issues regarding the occurrence, persistence, treatment, and transformations of pharmaceuticals in the environment and in drinking water and wastewater treatment systems. Acompilation of the recent literature, the book reviews advances in instrumentation and sample preparation techniques and includes an example of how risk assessment is conducted to investigate the fate and effects of pharmaceutical contaminants. Several chapters explore the behavior of pharmaceuticals in soil and the potential side effects of antibiotics on plants after uptake. Experts in drinking water and wastewater treatment systems present new findings on the effectiveness of current treatment practices to reduce the concentrations of pharmaceuticals at the source, providing new insights on how to better mitigate future problems brought about by emerging environmental contaminants. Contributing authors from academia, government, and industry provide a well-balanced multi-disciplinary perspective on the issues, discussing topics ranging from field studies documenting the occurrence of pharmaceuticals in environmental compartments, to laboratory studies determining the degradation kinetics and formation of by-products during treatment. The text discusses the factors that affect the environmental fate of pharmaceuticals in soil and water, facilitate the development of best management practices, and optimize treatment systems for removal of these compounds from the environment.

Filtration and Purification in the Biopharmaceutical Industry Third Edition

Filtration and Purification in the Biopharmaceutical Industry  Third Edition
Author: Maik W. Jornitz
Publsiher: CRC Press
Total Pages: 672
Release: 2019-06-26
ISBN 10: 1351675699
ISBN 13: 9781351675697
Language: EN, FR, DE, ES & NL

Filtration and Purification in the Biopharmaceutical Industry Third Edition Book Review:

Since sterile filtration and purification steps are becoming more prevalent and critical within medicinal drug manufacturing, the third edition of Filtration and Purification in the Biopharmaceutical Industry greatly expands its focus with extensive new material on the critical role of purification and advances in filtration science and technology. It provides state-of-the-science information on all aspects of bioprocessing including the current methods, processes, technologies and equipment. It also covers industry standards and regulatory requirements for the pharmaceutical and biopharmaceutical industries. The book is an essential, comprehensive source for all involved in filtration and purification practices, training and compliance. It describes such technologies as viral retentive filters, membrane chromatography, downstream processing, cell harvesting, and sterile filtration. Features: Addresses recent biotechnology-related processes and advanced technologies such as viral retentive filters, membrane chromatography, downstream processing, cell harvesting, and sterile filtration of medium, buffer and end product Presents detailed updates on the latest FDA and EMA regulatory requirements involving filtration and purification practices, as well as discussions on best practises in filter integrity testing Describes current industry quality standards and validation requirements and provides guidance for compliance, not just from an end-user perspective, but also supplier requirement It discusses the advantages of single-use process technologies and the qualification needs Sterilizing grade filtration qualification and process validation is presented in detail to gain the understanding of the regulatory needs The book has been compilated by highly experienced contributors in the field of pharmaceutical and biopharmaceutical processing. Each specific topic has been thoroughly examined by a subject matter expert.

Membrane Technology and Engineering for Water Purification

Membrane Technology and Engineering for Water Purification
Author: Rajindar Singh
Publsiher: Butterworth-Heinemann
Total Pages: 452
Release: 2014-09-25
ISBN 10: 0444634096
ISBN 13: 9780444634092
Language: EN, FR, DE, ES & NL

Membrane Technology and Engineering for Water Purification Book Review:

Membrane Technology and Engineering for Water Purification, Second Edition is written in a practical style with emphasis on: process description; key unit operations; systems design and costs; plant equipment description; equipment installation; safety and maintenance; process control; plant start-up; and operation and troubleshooting. It is supplemented by case studies and engineering rules-of-thumb. The author is a chemical engineer with extensive experience in the field, and his technical knowledge and practical know-how in the water purification industry are summarized succinctly in this new edition. This book will inform you which membranes to use in water purification and why, where and when to use them. It will help you to troubleshoot and improve performance and provides case studies to assist understanding through real-life examples. Membrane Technology section updated to include forward osmosis, electrodialysis, and diffusion dialysis Hybrid Membrane Systems expanded to cover zero liquid discharge, salt recovery and removal of trace contaminants Includes a new section on plant design, energy, and economics

Handbook of Validation in Pharmaceutical Processes

Handbook of Validation in Pharmaceutical Processes
Author: James P. Agalloco,Phil DeSantis,Anthony Grilli,Anthony Pavell
Publsiher: Unknown
Total Pages: 135
Release: 2022
ISBN 10: 9780367756062
ISBN 13: 0367756064
Language: EN, FR, DE, ES & NL

Handbook of Validation in Pharmaceutical Processes Book Review:

"Revised to reflect significant advances in pharmaceutical production and regulatory expectations, Handbook of Validation in Pharmaceutical Processes, Fourth Edition examines and blueprints every step of the validation process needed to remain compliant and competitive. This book blends the use of theoretical knowledge with recent technological advancements to achieve applied practical solutions. As the industry's leading source for validation of sterile pharmaceutical processes for more than 10 years, this greatly expanded work is a comprehensive analysis of all the fundamental elements of pharmaceutical and bio-pharmaceutical production processes. Handbook of Validation in Pharmaceutical Processes, Fourth Edition is essential for all global health care manufacturers and pharmaceutical industry professionals"--

Water Purification

Water Purification
Author: Alexandru Grumezescu
Publsiher: Academic Press
Total Pages: 772
Release: 2016-12-28
ISBN 10: 0128043717
ISBN 13: 9780128043714
Language: EN, FR, DE, ES & NL

Water Purification Book Review:

Water Purification, a volume in the Nanotechnology in the Food Industry series, provides an in-depth review of the current technologies and emerging application of nanotechnology in drinking water purification, also presenting an overview of the common drinking water contaminants, such as heavy metals, organics, microorganisms, pharmaceuticals, and their occurrences in drinking water sources. As the global water crisis has motivated the industry to look for alternative water supplies, nanotechnology presents significant potential for utilizing previously unacceptable water sources. This books explores the practical methodologies for transforming water using nanotechnologies, and is a comprehensive reference to a wide audience of food science research professionals, professors, and students who are doing research in this field. Includes the most up-to-date information on nanotechnology applications and research methods for water purification and treatment Presents applications of nanotechnology and engineered nanomaterials in drinking water purification to improve efficiency and reduce cost Provides water purification research methods that are important to water quality, including precipitation, adsorption, membrane separation, and ion exchange Covers the potential risks of nanotechnology, such as the toxicological effects of engineered nanomaterials in water and how to minimize risks based on research studies

Biocontamination Control for Pharmaceuticals and Healthcare

Biocontamination Control for Pharmaceuticals and Healthcare
Author: Tim Sandle
Publsiher: Academic Press
Total Pages: 374
Release: 2018-11-30
ISBN 10: 0128149124
ISBN 13: 9780128149126
Language: EN, FR, DE, ES & NL

Biocontamination Control for Pharmaceuticals and Healthcare Book Review:

Biocontamination Control for Pharmaceuticals and Healthcare outlines a biocontamination strategy that tracks bio-burden control and reduction at each transition in classified areas of a facility. This key part of controlling risk escalation can lead to the contamination of medicinal products, hence necessary tracking precautions are essential. Regulatory authorities have challenged pharmaceutical companies, healthcare providers, and those in manufacturing practice to adopt a holistic approach to contamination control. New technologies are needed to introduce barriers between personnel and the environment, and to provide a rapid and more accurate assessment of risk. This book offers guidance on building a complete biocontamination strategy. Provides the information necessary for a facility to build a complete biocontamination strategy Helps facilities understand the main biocontamination risks to medicinal products Assists the reader in navigating regulatory requirements Provides insight into developing an environmental monitoring program Covers the types of rapid microbiological monitoring methods now available, as well as current legislation

Pharmaceutical Residues in Freshwater Hazards and Policy Responses

Pharmaceutical Residues in Freshwater  Hazards and Policy Responses
Author: Organisation for Economic Co-Operation and Development (OECD)
Publsiher: IWA Publishing
Total Pages: 136
Release: 2020-07-15
ISBN 10: 1789061814
ISBN 13: 9781789061819
Language: EN, FR, DE, ES & NL

Pharmaceutical Residues in Freshwater Hazards and Policy Responses Book Review:

This report calls for a better understanding of the effects of pharmaceutical residues in the environment, greater international collaboration and accountability distribution, and policy actions to prevent and remedy emerging concerns. Laboratory and field tests show traces of oral contraceptives causing the feminisation of fish and amphibians, and residues of psychiatric drugs altering fish behaviour. Antimicrobial resistance, linked to the overuse of antibiotics, has rapidly escalated into a global health crisis. Unless adequate measures are taken to manage the risks, pharmaceutical residues will increasingly be released into the environment as ageing populations, advances in healthcare, and intensification of meat and fish production spur the demand for pharmaceuticals worldwide. The report outlines a collective, life‑cycle approach to managing pharmaceuticals in the environment. A policy mix of source‑directed, use‑orientated and end‑of‑pipe measures, involving several policy sectors, can help to improve health and protect the environment.

Biofouling and Biocorrosion in Industrial Water Systems

Biofouling and Biocorrosion in Industrial Water Systems
Author: Hans-Curt Flemming,Gill G. Geesey
Publsiher: Springer Science & Business Media
Total Pages: 220
Release: 2012-12-06
ISBN 10: 3642765432
ISBN 13: 9783642765438
Language: EN, FR, DE, ES & NL

Biofouling and Biocorrosion in Industrial Water Systems Book Review:

Microbial growth and contamination ("Biofouling") in water systems represents a significant threat to the quality of waters produced for the microelectronic, pharmaceutical, petroleum, paper, food and other manufacturing industries. Biofouling can lead to biologically induced corrosion ("Biocorrosion"), which can cause severe damage to the equipment. Both biofouling and biocorrosion are frequently not recognized in time, underestimated, or linked with the wrong causes. The book represents a new approach by introducing biofilm properties and dynamics as basic principles of biofouling and biocorrosion, thus providing a better understanding and the means of fighting the undesired effects of biofilms. The most important features are: Case histories of biofouling in water treatment.- Detection and monitoring of biofouling.- Reverse osmosis membrane biofouling.- Biocide efficacy and biofouling control.- Plant design considerations for preventing biofouling.- Case histories of biocorrosion.- Detection, monitoring, control and prevention of biocorrosion.- Fundamentals of biofouling and biocorrosion mechanisms.

Pharmaceutical Water

Pharmaceutical Water
Author: William V. Collentro
Publsiher: CRC Press
Total Pages: 478
Release: 2010-12-21
ISBN 10: 9781420077827
ISBN 13: 1420077821
Language: EN, FR, DE, ES & NL

Pharmaceutical Water Book Review:

A major new work on all aspects of water, the most used raw material ingredient in the pharmaceutical and biotechnology industries—used as an excipient in pharmaceutical formulations, as a cleaning agent, and as a separately packaged product diluent. Drawing on the author’s extensive field experience with more than 400 pharmaceutical and related water purification systems, the text’s numerous case studies illuminate the best and worst of water system design and operation. The expanded Second Edition also includes new chapters that discuss: passivation and electropolishing rouging ozone systems and accessories USP purified water and water for injection individual component process and instrumentation diagram (P&IDs) with control interface documentation and specification requirements systems installation, start-up, and commissioning

Pharmaceuticals in the Environment

Pharmaceuticals in the Environment
Author: Klaus Kümmerer
Publsiher: Springer Science & Business Media
Total Pages: 521
Release: 2008-10-10
ISBN 10: 3540746641
ISBN 13: 9783540746645
Language: EN, FR, DE, ES & NL

Pharmaceuticals in the Environment Book Review:

Following the success of the first edition, this pioneering study of pharmaceuticals in the environment has been updated and greatly extended. It includes the status of research on pharmaceuticals in soil, with attention to terrestrial and aquatic environments as well as new substance categories such as tetracylines and chinolones and the latest results concerning contamination of the environment and risk reduction.

Validation of Pharmaceutical Processes

Validation of Pharmaceutical Processes
Author: James P. Agalloco,Frederick J. Carleton
Publsiher: CRC Press
Total Pages: 760
Release: 2007-09-25
ISBN 10: 1420019791
ISBN 13: 9781420019797
Language: EN, FR, DE, ES & NL

Validation of Pharmaceutical Processes Book Review:

Completely revised and updated to reflect the significant advances in pharmaceutical production and regulatory expectations, this third edition of Validation of Pharmaceutical Processes examines and blueprints every step of the validation process needed to remain compliant and competitive. The many chapters added to the prior compilation examine va

Sterile Pharmaceutical Products

Sterile Pharmaceutical Products
Author: KennethE. Avis
Publsiher: Routledge
Total Pages: 428
Release: 2018-03-29
ISBN 10: 1351413864
ISBN 13: 9781351413862
Language: EN, FR, DE, ES & NL

Sterile Pharmaceutical Products Book Review:

Sterile Pharmaceutical Products: Process Engineering Applications addresses the key concepts and applications of the sterile pharmaceutical manufacturing industry. It covers elements of the design, installation, validation, and usage of critical processes associated with sterile product manufacture. From water systems to clean-in-place systems, to sterile powder handling and robotic applications in sterile production environments, this book addresses the issues of system implementation, integration, and operations. Written by recognized experts and peer reviewed for accuracy, all chapters include references to supplemental resources and numerous illustrations.

Good Design Practices for GMP Pharmaceutical Facilities

Good Design Practices for GMP Pharmaceutical Facilities
Author: Terry Jacobs,Andrew A. Signore
Publsiher: CRC Press
Total Pages: 536
Release: 2016-08-19
ISBN 10: 1482258919
ISBN 13: 9781482258912
Language: EN, FR, DE, ES & NL

Good Design Practices for GMP Pharmaceutical Facilities Book Review:

This revised publication serves as a handy and current reference for professionals engaged in planning, designing, building, validating and maintaining modern cGMP pharmaceutical manufacturing facilities in the U.S. and internationally. The new edition expands on facility planning, with a focus on the ever-growing need to modify existing legacy facilities, and on current trends in pharmaceutical manufacturing which include strategies for sustainability and LEED building ratings. All chapters have been re-examined with a fresh outlook on current good design practices.

Microbial Contamination Control in Parenteral Manufacturing

Microbial Contamination Control in Parenteral Manufacturing
Author: Kevin Williams
Publsiher: CRC Press
Total Pages: 764
Release: 2004-05-20
ISBN 10: 113553621X
ISBN 13: 9781135536213
Language: EN, FR, DE, ES & NL

Microbial Contamination Control in Parenteral Manufacturing Book Review:

This reference surveys emerging trends, concepts, and procedures used in the characterization and control of contaminants; the sterile production of traditional drugs and biologics; the design, construction, and validation of new parenteral facilities; and the monitoring of clean environments-vividly illustrating the routes by which products, proce

Practical Pharmaceutical Engineering

Practical Pharmaceutical Engineering
Author: Gary Prager
Publsiher: Wiley
Total Pages: 576
Release: 2018-12-18
ISBN 10: 0470410329
ISBN 13: 9780470410325
Language: EN, FR, DE, ES & NL

Practical Pharmaceutical Engineering Book Review:

A practical guide to all key the elements of pharmaceuticals and biotech manufacturing and design Engineers working in the pharmaceutical and biotech industries are routinely called upon to handle operational issues outside of their fields of expertise. Traditionally the competencies required to fulfill those tasks were achieved piecemeal, through years of self-teaching and on-the-job experience—until now. Practical Pharmaceutical Engineering provides readers with the technical information and tools needed to deal with most common engineering issues that can arise in the course of day-to-day operations of pharmaceutical/biotech research and manufacturing. Engineers working in pharma/biotech wear many hats. They are involved in the conception, design, construction, and operation of research facilities and manufacturing plants, as well as the scale-up, manufacturing, packaging, and labeling processes. They have to implement FDA regulations, validation assurance, quality control, and Good Manufacturing Practices (GMP) compliance measures, and to maintain a high level of personal and environmental safety. This book provides readers from a range of engineering specialties with a detailed blueprint and the technical knowledge needed to tackle those critical responsibilities with confidence. At minimum, after reading this book, readers will have the knowledge needed to constructively participate in contractor/user briefings. Provides pharmaceutical industry professionals with an overview of how all the parts fit together and a level of expertise that can take years of on-the-job experience to acquire Addresses topics not covered in university courses but which are crucial to working effectively in the pharma/biotech industry Fills a gap in the literature, providing important information on pharmaceutical operation issues required for meeting regulatory guidelines, plant support design, and project engineering Covers the basics of HVAC systems, water systems, electric systems, reliability, maintainability, and quality assurance, relevant to pharmaceutical engineering Practical Pharmaceutical Engineering is an indispensable “tool of the trade” for chemical engineers, mechanical engineers, and pharmaceutical engineers employed by pharmaceutical and biotech companies, engineering firms, and consulting firms. It also is a must-read for engineering students, pharmacy students, chemistry students, and others considering a career in pharmaceuticals.

Testing and Balancing HVAC Air and Water Systems Fourth Edition

Testing and Balancing HVAC Air and Water Systems  Fourth Edition
Author: Samuel C. Sugarman
Publsiher: Fairmont Press
Total Pages: 325
Release: 2006-02-17
ISBN 10: 1928374650XXX
ISBN 13: UOM:39015063358157
Language: EN, FR, DE, ES & NL

Testing and Balancing HVAC Air and Water Systems Fourth Edition Book Review:

This fully revised and updated edition of this classic bestselling reference provides all the information needed to evaluate and balance the air and water sides of any HVAC system. The third edition adds new chapters on testing and balancing clean rooms and HVAC system commissioning. The book addresses every aspect of testing, adjusting and balancing, including all types of instruments required and specific methods to adjust constant volume, single zone, dual duct, induction, and variable air volume systems. The author provides complete details for the full scope of system components, including fans, pumps, motors, drives, and electricity, as well as for balancing devices and instrument usage. The book also includes all necessary equations and a variety of useful conversion tables.

Advances and Challenges in Pharmaceutical Technology

Advances and Challenges in Pharmaceutical Technology
Author: Amit Kumar Nayak,Kunal Pal,Indranil Banerjee,Samarendra Maji,Upendranath Nanda
Publsiher: Academic Press
Total Pages: 568
Release: 2021-02-09
ISBN 10: 0128203005
ISBN 13: 9780128203002
Language: EN, FR, DE, ES & NL

Advances and Challenges in Pharmaceutical Technology Book Review:

Advances and Challenges in Pharmaceutical Technology: Materials, Process Development and Drug Delivery Strategies examines recent advancements in pharmaceutical technology. The book discusses common formulation strategies, including the use of tools for statistical formulation optimization, Quality by design (QbD), process analytical technology, and the uses of various pharmaceutical biomaterials, including natural polymers, synthetic polymers, modified natural polymers, bioceramics, and other bioinorganics. In addition, the book covers rapid advancements in the field by providing a thorough understanding of pharmaceutical processes, formulation developments, explorations, and exploitation of various pharmaceutical biomaterials to formulate pharmaceutical dosage forms. Provides extensive information and analysis on recent advancements in the field of pharmaceutical technology Includes contributions from global leaders and experts in academia, industry and regulatory agencies Uses high quality illustrations, flow charts and tables to explain concepts and text to readers, along with practical examples and research case studies

Bioprocessing Piping and Equipment Design

Bioprocessing Piping and Equipment Design
Author: William M. (Bill) Huitt
Publsiher: John Wiley & Sons
Total Pages: 544
Release: 2016-09-23
ISBN 10: 1119284252
ISBN 13: 9781119284253
Language: EN, FR, DE, ES & NL

Bioprocessing Piping and Equipment Design Book Review:

The only comprehensive and authoritative reference guide to the ASME Bioprocessing Piping and Equipment (BPE) standard This is a companion guide to the ASME Bioprocessing Piping and Equipment (BPE) Standard and explains what lies behind many of the requirements and recommendations within that industry standard. Following an introductory narrative to the Standard's early history, industry related codes and standards are explained; the design and engineering aspects cover construction materials, both metallic and nonmetallic; then components, fabrication, assembly and installation of piping systems are explored. Examination, Inspection and Testing then precede the ASME BPE certification process, concluding with a discussion on system design. The author draws on many years' experience and insights from first-hand involvement in the field of industrial piping design, engineering, construction, and management, which includes the bioprocessing industry. The reader will learn why dimensions and tolerances, process instrumentation, and material selection play such an integral part in the manufacture of components and instrumentation. This easy to understand and navigate guide will assist engineers (design, piping, chemical, etc.) who need to understand the basis for much of the Standard’s content, as do the contractors and inspectors who have to meet and validate compliance with the BPE Standard.