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

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.

Handbook of Validation in Pharmaceutical Processes Fourth Edition

Handbook of Validation in Pharmaceutical Processes  Fourth Edition
Author: James Agalloco,Phil DeSantis,Anthony Grilli,Anthony Pavell
Publsiher: CRC Press
Total Pages: 1061
Release: 2021-10-28
ISBN 10: 1000436012
ISBN 13: 9781000436013
Language: EN, FR, DE, ES & NL

Handbook of Validation in Pharmaceutical Processes Fourth Edition 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. Key Features: Provides an in-depth discussion of recent advances in sterilization Identifies obstacles that may be encountered at any stage of the validation program, and suggests the newest and most advanced solutions Explores distinctive and specific process steps, and identifies critical process control points to reach acceptable results New chapters include disposable systems, combination products, nano-technology, rapid microbial methods, contamination control in non-sterile products, liquid chemical sterilization, and medical device manufacture

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: 654
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.

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 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

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.

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

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.

Advances in Control and Automation of Water Systems

Advances in Control and Automation of Water Systems
Author: Kaveh Hariri Asli,Faig Bakhman Ogli Naghiyev,Reza Khodaparast Haghi,Hossien Hariri Asli
Publsiher: CRC Press
Total Pages: 190
Release: 2012-07-23
ISBN 10: 1926895223
ISBN 13: 9781926895222
Language: EN, FR, DE, ES & NL

Advances in Control and Automation of Water Systems Book Review:

Control and automation of water systems in one of the branches of fluid mechanics and hydraulics that uses numerical methods and algorithms to solve and analyze problems that involve fluid flows. Computers are used to perform the millions of calculations required to simulate the interaction of liquids and gases with surfaces defined by boundary conditions. Advances in Control and Automation of Water Systems presents topical research in the study of control and automation of water systems. The editors use the simulation of a water hammer (or fluid hammer) as the basis for demonstrating computational techniques used for the processing and automation of water systems. The simulation shows and explains a variety of data analysis techniques and complex calculations that involve many elements of water systems, such as flow minimum and maximum pressure automation heat and mass transfer predicting failure and more. This book provides a broad understanding of the main computational techniques used for processing control and automation of water systems. The theoretical background to a number of techniques is introduced, and general data analysis techniques and examining the application of techniques in an industrial setting, including current practices and current research, are considered. The book also provides practical experience of commercially available systems and includes a small-scale water systems related projects. This book provides innovative chapters on the growth of educational, scientific, and industrial research activities among mechanical engineers and international academia in the water industry. New methods and novel applications of existing methods are discussed that further the understanding of the structural behavior of new and advanced systems. This book presents significant research reporting new methodologies and important applications in the fields of automation and control as well as the latest coverage of chemical databases and the development of new computational methods and efficient algorithms for hydraulic software and mechanical engineering. The research and development presented in the book will have significant potential applications in several disciplines of hydraulic and mechanical engineering.

Principles of Parenteral Solution Validation

Principles of Parenteral Solution Validation
Author: Igor Gorsky,Harold S. Baseman
Publsiher: Academic Press
Total Pages: 298
Release: 2019-11-27
ISBN 10: 012809446X
ISBN 13: 9780128094464
Language: EN, FR, DE, ES & NL

Principles of Parenteral Solution Validation Book Review:

Principles of Parenteral Solution Validation: A Practical Lifecycle Approach covers all aspects involved in the development and process validation of a parenteral product. By using a lifecycle approach, this book discusses the latest technology, compliance developments, and regulatory considerations and trends, from process design, to divesting. As part of the Expertise in Pharmaceutical Process Technology series edited by Michael Levin, this book incorporates numerous case studies and real-world examples that address timely problems and offer solutions to the daily challenges facing practitioners in this area. Discusses international and domestic regulatory considerations in every section Features callout boxes that contain points-of-interest for each segment of the audience so readers can quickly find their interests and needs Contains important topics, including risk management, the preparation and execution of properly designed studies, scale-up and technology transfer activities, problem-solving, and more

Water Properties in Food Health Pharmaceutical and Biological Systems

Water Properties in Food  Health  Pharmaceutical and Biological Systems
Author: David S. Reid,Tanaboon Sajjaanantakul,Peter J. Lillford,Sanguansri Charoenrein
Publsiher: John Wiley & Sons
Total Pages: 804
Release: 2010-11-29
ISBN 10: 9780470959565
ISBN 13: 0470959568
Language: EN, FR, DE, ES & NL

Water Properties in Food Health Pharmaceutical and Biological Systems Book Review:

This title focuses on the comprehension of the properties of water in foods, enriched by the approaches from polymer and materials sciences, and by the advances of analytical techniques. The International Symposium on the Properties of Water (ISOPOW) promotes the exchange of knowledge between scientists involved in the study of food materials and scientists interested in water from a more basic point of view and the dialogue between academic and industrial scientists/technologists. This comprehensive book covers the topics presented at the 10th ISOPOW held in Bangkok, Thailand in 2007, including water dynamics in various systems, the role of water in functional food and nano-structured biomaterials. Special features include: Latest findings in the properties of water in food, pharmaceutical and biological systems Coverage of the 10th International Symposium on the Properties of Water (ISOPOW) Includes water dynamics, water in foods stability, and water in micro and nano-structured food and biomaterials Reflects the vast array of research and applications of water world wide

High purity Water Preparation for the Semiconductor Pharmaceutical and Power Industries

High purity Water Preparation for the Semiconductor  Pharmaceutical  and Power Industries
Author: Theodore H. Meltzer
Publsiher: Tall Oaks Pub
Total Pages: 833
Release: 1993-01-01
ISBN 10: 9780927188029
ISBN 13: 0927188023
Language: EN, FR, DE, ES & NL

High purity Water Preparation for the Semiconductor Pharmaceutical and Power Industries Book Review:

Pharmaceutical Microbiology

Pharmaceutical Microbiology
Author: Tim Sandle
Publsiher: Woodhead Publishing
Total Pages: 316
Release: 2015-10-09
ISBN 10: 0081000448
ISBN 13: 9780081000441
Language: EN, FR, DE, ES & NL

Pharmaceutical Microbiology Book Review:

Pharmaceutical Microbiology: Essentials for Quality Assurance and Quality Control presents that latest information on protecting pharmaceutical and healthcare products from spoilage by microorganisms, and protecting patients and consumers. With both sterile and non-sterile products, the effects can range from discoloration to the potential for fatality. The book provides an overview of the function of the pharmaceutical microbiologist and what they need to know, from regulatory filing and GMP, to laboratory design and management, and compendia tests and risk assessment tools and techniques. These key aspects are discussed through a series of dedicated chapters, with topics covering auditing, validation, data analysis, bioburden, toxins, microbial identification, culture media, and contamination control. Contains the applications of pharmaceutical microbiology in sterile and non-sterile products Presents the practical aspects of pharmaceutical microbiology testing Provides contamination control risks and remediation strategies, along with rapid microbiological methods Includes bioburden, endotoxin, and specific microbial risks Highlights relevant case studies and risk assessment scenarios

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

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.

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

Management of Animal Care and Use Programs in Research Education and Testing

Management of Animal Care and Use Programs in Research  Education  and Testing
Author: Robert H. Weichbrod,Gail A. (Heidbrink) Thompson,John N. Norton
Publsiher: CRC Press
Total Pages: 872
Release: 2017-09-07
ISBN 10: 1351648225
ISBN 13: 9781351648226
Language: EN, FR, DE, ES & NL

Management of Animal Care and Use Programs in Research Education and Testing Book Review:

AAP Prose Award Finalist 2018/19 Management of Animal Care and Use Programs in Research, Education, and Testing, Second Edition is the extensively expanded revision of the popular Management of Laboratory Animal Care and Use Programs book published earlier this century. Following in the footsteps of the first edition, this revision serves as a first line management resource, providing for strong advocacy for advancing quality animal welfare and science worldwide, and continues as a valuable seminal reference for those engaged in all types of programs involving animal care and use. The new edition has more than doubled the number of chapters in the original volume to present a more comprehensive overview of the current breadth and depth of the field with applicability to an international audience. Readers are provided with the latest information and resource and reference material from authors who are noted experts in their field. The book: - Emphasizes the importance of developing a collaborative culture of care within an animal care and use program and provides information about how behavioral management through animal training can play an integral role in a veterinary health program - Provides a new section on Environment and Housing, containing chapters that focus on management considerations of housing and enrichment delineated by species - Expands coverage of regulatory oversight and compliance, assessment, and assurance issues and processes, including a greater discussion of globalization and harmonizing cultural and regulatory issues - Includes more in-depth treatment throughout the book of critical topics in program management, physical plant, animal health, and husbandry. Biomedical research using animals requires administrators and managers who are knowledgeable and highly skilled. They must adapt to the complexity of rapidly-changing technologies, balance research goals with a thorough understanding of regulatory requirements and guidelines, and know how to work with a multi-generational, multi-cultural workforce. This book is the ideal resource for these professionals. It also serves as an indispensable resource text for certification exams and credentialing boards for a multitude of professional societies Co-publishers on the second edition are: ACLAM (American College of Laboratory Animal Medicine); ECLAM (European College of Laboratory Animal Medicine); IACLAM (International Colleges of Laboratory Animal Medicine); JCLAM (Japanese College of Laboratory Animal Medicine); KCLAM (Korean College of Laboratory Animal Medicine); CALAS (Canadian Association of Laboratory Animal Medicine); LAMA (Laboratory Animal Management Association); and IAT (Institute of Animal Technology).

Pharmaceuticals and Personal Care Products Waste Management and Treatment Technology

Pharmaceuticals and Personal Care Products  Waste Management and Treatment Technology
Author: Majeti Narasimha Vara Prasad,Meththika Vithanage,Atya Kapley
Publsiher: Butterworth-Heinemann
Total Pages: 506
Release: 2019-04-04
ISBN 10: 0128165901
ISBN 13: 9780128165904
Language: EN, FR, DE, ES & NL

Pharmaceuticals and Personal Care Products Waste Management and Treatment Technology Book Review:

Pharmaceuticals and Personal Care Products Waste Management and Treatment Technology: Emerging Contaminants and Micro Pollutants provides the tools and techniques for identifying these contaminates and applying the most effective technology for their remediation, recovery and treatment. The consumption of pharmaceuticals and personal care products (PPCPs) has grown significantly over the last 35 years, thus increasing their potential risk to the environment. As PPCPs are very difficult to detect and remove using conventional wastewater treatment methods, this book provides solutions to a growing problem. Includes sampling, analytical and characterization methods and technology for detecting PPCPs in the environment Provides advanced treatment and disposal technologies for the removal of PPCPs from wastewater, surface water, landfills and septic systems Examines the pathways of PPCPs into the environment

Standard Methods for the Examination of Water and Wastewater

Standard Methods for the Examination of Water and Wastewater
Author: American Public Health Association
Publsiher: Unknown
Total Pages: 135
Release: 1915
ISBN 10: 1928374650XXX
ISBN 13: UOM:39015068248015
Language: EN, FR, DE, ES & NL

Standard Methods for the Examination of Water and Wastewater Book Review:

"The signature undertaking of the Twenty-Second Edition was clarifying the QC practices necessary to perform the methods in this manual. Section in Part 1000 were rewritten, and detailed QC sections were added in Parts 2000 through 7000. These changes are a direct and necessary result of the mandate to stay abreast of regulatory requirements and a policy intended to clarify the QC steps considered to be an integral part of each test method. Additional QC steps were added to almost half of the sections."--Pref. p. iv.