Biomedical Devices

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Publisher : John Wiley & Sons
ISBN 13 : 1119267048
Total Pages : 225 pages
Book Rating : 4.1/5 (192 download)

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Book Synopsis Biomedical Devices by : Tugrul Özel

Download or read book Biomedical Devices written by Tugrul Özel and published by John Wiley & Sons. This book was released on 2016-09-12 with total page 225 pages. Available in PDF, EPUB and Kindle. Book excerpt: Biomedical Devices: Design, Prototyping, and Manufacturing features fundamental discussions of all facets of materials processing and manufacturing processes across a wide range of medical devices and artificial tissues. Represents the first compilation of information on the design, prototyping, and manufacture of medical devices into one volume Offers in-depth coverage of medical devices, beginning with an introductory overview through to the design, manufacture, and applications Features examples of a variety of medical applications of devices, including biopsy micro forceps, micro-needle arrays, wrist implants, spinal spacers, and fixtures Provides students, doctors, scientists, and technicians interested in the development and applications of medical devices the ideal reference source

Nanoparticles in the Water Cycle

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Publisher : Springer Science & Business Media
ISBN 13 : 3642103189
Total Pages : 243 pages
Book Rating : 4.6/5 (421 download)

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Book Synopsis Nanoparticles in the Water Cycle by : Fritz H. Frimmel

Download or read book Nanoparticles in the Water Cycle written by Fritz H. Frimmel and published by Springer Science & Business Media. This book was released on 2010-07-15 with total page 243 pages. Available in PDF, EPUB and Kindle. Book excerpt: As nanotechnology enters everyday life, engineered nanoparticles (ENP) will find their way into nature, including surface and groundwater. Here, distinguished experts of water chemistry present dedicated methods for the analysis of nanoparticles in the aquatic environment, their distribution and fate. This includes the influence of complex matrices such as wastewater, brown water with natural organic matter (NOM), and high salt concentrations as well as available and future standardized methods. The background of geogenic, natural nanoparticles is considered in a discussion of known environmental effects, including strategies to test for potential effects on human and environmental health.

Biocompatibility of Dental Materials

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Publisher : Springer Science & Business Media
ISBN 13 : 3540777822
Total Pages : 392 pages
Book Rating : 4.5/5 (47 download)

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Book Synopsis Biocompatibility of Dental Materials by : Gottfried Schmalz

Download or read book Biocompatibility of Dental Materials written by Gottfried Schmalz and published by Springer Science & Business Media. This book was released on 2008-10-10 with total page 392 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book provides a comprehensive and scientifically based overview of the biocompatibility of dental materials. Up-to-date concepts of biocompatibility assessment are presented, as well as information on almost all material groups used in daily dentistry practice. Furthermore, special topics of clinical relevance (e.g,, environmental and occupational hazards and the diagnosis of adverse effects) are covered. The book will: improve the reader’s ability to critically analyze information provided by manufacturers supply a better understanding of the biocompatibility of single material groups, which will help the reader choose the most appropriate materials for any given patient and thus prevent adverse effects from developing provide insights on how to conduct objective, matter-of-fact discussions with patients about the materials to be used in dental procedures advise readers, through the use of well-documented concepts, on how to treat patients who claim adverse effects from dental materials feature clinical photographs that will serve as a reference when analyzing clinical symptoms, such as oral mucosa reactions.

Biological Evaluation of Medical Devices

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Publisher :
ISBN 13 :
Total Pages : 28 pages
Book Rating : 4.3/5 (91 download)

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Book Synopsis Biological Evaluation of Medical Devices by : International Organization for Standardization

Download or read book Biological Evaluation of Medical Devices written by International Organization for Standardization and published by . This book was released on 2006 with total page 28 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Plastics in Medical Devices

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Author :
Publisher : William Andrew
ISBN 13 : 0323851274
Total Pages : 525 pages
Book Rating : 4.3/5 (238 download)

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Book Synopsis Plastics in Medical Devices by : Vinny R. Sastri

Download or read book Plastics in Medical Devices written by Vinny R. Sastri and published by William Andrew. This book was released on 2021-11-24 with total page 525 pages. Available in PDF, EPUB and Kindle. Book excerpt: Plastics in Medical Devices: Properties, Requirements, and Applications, Third Edition provides a comprehensive overview on the main types of plastics used in medical device applications. The book focuses on the applications and properties that are most important in medical device design, such as chemical resistance, sterilization capability and biocompatibility. The roles of additives, stabilizers and fillers as well as the synthesis and production of polymers are covered and backed up with a wealth of data tables. The book also covers other key aspects in detail, including regulations, compliance, purchasing controls and supplier controls, and process validation. This updated edition has been thoroughly revised with regard to new plastic materials, applications and requirements. This is a valuable resource for engineers, scientists and managers involved in the design and manufacture of medical devices. - Presents detailed coverage of commercially available plastics used in medical device applications, organized by polymer type and supported by data - Includes up-to-date regulatory requirements and practical information on purchasing and supplier controls, process validation and risk management - Supports the development, marketing and commercialization of medical devices and materials for use in medical devices

Biocompatibility and Performance of Medical Devices

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Author :
Publisher : Woodhead Publishing
ISBN 13 : 0081026447
Total Pages : 592 pages
Book Rating : 4.0/5 (81 download)

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Book Synopsis Biocompatibility and Performance of Medical Devices by : Jean-Pierre Boutrand

Download or read book Biocompatibility and Performance of Medical Devices written by Jean-Pierre Boutrand and published by Woodhead Publishing. This book was released on 2019-11-21 with total page 592 pages. Available in PDF, EPUB and Kindle. Book excerpt: Biocompatibility and Performance of Medical Devices, Second Edition, provides an understanding of the biocompatibility and performance tests for ensuring that biomaterials and medical devices are safe and will perform as expected in the biological environment. Sections cover key concepts and challenges faced in relation to biocompatibility in medical devices, discuss the evaluation and characterization of biocompatibility in medical devices, describe preclinical performance studies for bone, dental and soft tissue implants, and provide information on the regulation of medical devices in the European Union, Japan and China. The book concludes with a review of histopathology principles for biocompatibility and performance studies. - Presents diverse insights from experts in government, industry and academia - Delivers a comprehensive overview of testing and interpreting medical device performance - Expanded to include new information, including sections on managing extractables, accelerating and simplifying medical device development through screening and alternative biocompatibility methods, and quality strategies which fasten device access to market

Hemocompatibility of Biomaterials for Clinical Applications

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Publisher : Woodhead Publishing
ISBN 13 : 0081004990
Total Pages : 486 pages
Book Rating : 4.0/5 (81 download)

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Book Synopsis Hemocompatibility of Biomaterials for Clinical Applications by : Christopher Siedlecki

Download or read book Hemocompatibility of Biomaterials for Clinical Applications written by Christopher Siedlecki and published by Woodhead Publishing. This book was released on 2018-03-05 with total page 486 pages. Available in PDF, EPUB and Kindle. Book excerpt: Hemocompatibility of Biomaterials for Clinical Applications: Blood-Biomaterials Interactions summarizes the state-of-the-art on this important subject. The first part of the book reviews the latest research on blood composition and response, mechanisms of coagulation, test standards and methods. Next, the book assesses techniques for modifying biomaterial surfaces and developing coatings to improve hemocompatibility. In the final sections, users will find discussions on ways to improve the hemocompatibility of particular classes of biomaterials and a review of methods for improving medical devices. - Provides comprehensive information on the fundamentals of hemocompatibility and new technologies - Combines research in the biomaterials field in a digestible format for clinical applications - Provides a complete overview biomaterials in current use and test methods

Standardisation in Cell and Tissue Engineering

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Author :
Publisher : Elsevier
ISBN 13 : 0857098721
Total Pages : 282 pages
Book Rating : 4.8/5 (57 download)

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Book Synopsis Standardisation in Cell and Tissue Engineering by : V Salih

Download or read book Standardisation in Cell and Tissue Engineering written by V Salih and published by Elsevier. This book was released on 2013-07-31 with total page 282 pages. Available in PDF, EPUB and Kindle. Book excerpt: The increased use of biodegradable synthetic or natural scaffolds combined with cells and/or biological molecules, in order to create functional replacement tissue in a damaged tissue site, has led to the need for the development of 'best practice' methods in the area of tissue engineering to help ensure the creation of safe, high quality products. Standardisation in cell and tissue engineering introduces concepts and current practice in the field of cell and tissue engineering to a wide audience and aims to provide awareness of the importance of standardisation in this area while suggesting directions for further investigation.Part one provides an overview of methods for cell and tissue engineering and includes chapters on the fundamentals of cell and matrix biology for tissue engineering, 3D collagen biomatrix development, and control and vascularisation of tissue-engineered constructs. Part two begins with a chapter exploring the methods and protocols of standardisation in cell and tissue engineering before moving on to highlight issues of quality control in cell and tissue engineering, standardised chemical analysis and testing of biomaterials and principles of good laboratory practice (GLP) for in vitro cell culture applications.Standardisation in cell and tissue engineering is a standard reference for leading research groups, government agencies, regulatory bodies, and researchers and technicians at all levels across the whole range of disciplines using cell culture within the pharmaceutical, biotechnology and biomedical industries. - Introduces concepts and current practice in the field of cell and tissue engineering - Highlights the importance of standardisation in cell and tissue engineering and suggests directions for further investigation - Explores methods and protocols of standardisation in cell and tissue engineering and issues of quality control in cell and tissue engineering

The Role of the Study Director in Nonclinical Studies

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Author :
Publisher : John Wiley & Sons
ISBN 13 : 1118370392
Total Pages : 568 pages
Book Rating : 4.1/5 (183 download)

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Book Synopsis The Role of the Study Director in Nonclinical Studies by : William J. Brock

Download or read book The Role of the Study Director in Nonclinical Studies written by William J. Brock and published by John Wiley & Sons. This book was released on 2014-06-03 with total page 568 pages. Available in PDF, EPUB and Kindle. Book excerpt: A single-source reference with a broad and holistic overview of nonclinical studies, this book offers critical training material and describes regulations of nonclinical testing through guidelines, models, case studies, practical examples, and worldwide perspectives. The book: Provides a complete overview of nonclinical study organization, conduct, and reporting and describes the roles and responsibilities of a Study Director to manage an effective study Covers regulatory and scientific concepts, including international testing and Good Laboratory Practice (GLP), compliance with guidelines, and animal models Features a concluding chapter that compiles case studies / lessons learned from those that have served as a Study Director for many years Addresses the entire spectrum of nonclinical testing, making it applicable to those in the government, laboratories and those actively involved in in all sectors of industry

Testing Tribocorrosion of Passivating Materials Supporting Research and Industrial Innovation

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Author :
Publisher : Routledge
ISBN 13 : 1351546937
Total Pages : 272 pages
Book Rating : 4.3/5 (515 download)

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Book Synopsis Testing Tribocorrosion of Passivating Materials Supporting Research and Industrial Innovation by : Jean-Pierre Celis

Download or read book Testing Tribocorrosion of Passivating Materials Supporting Research and Industrial Innovation written by Jean-Pierre Celis and published by Routledge. This book was released on 2017-07-05 with total page 272 pages. Available in PDF, EPUB and Kindle. Book excerpt: This first edition of Testing Tribocorrosion of Passivating Materials Supporting Research and Industrial Innovation: A Handbook treats in a clear, concise, and practical manner an important material degradation and protection matter. It is designed as a handbook and provides a well structured approach of the basics needed to investigate the tribocorrosion behavior of passivating materials, and to conduct in a correct way a laboratory investigation on it. It provides answers on practical and theoretical approaches of tribocorrosion phenomena to engineers and medical persons involved with material assemblies subjected to aggressive environmental and mechanical conditions. For academic researchers it is a pertinent tool assisting them in how they can perform a tribocorrosion investigation and obtain results that are correctly interpreted and can be exchanged. Different parts of the book are illustrated with practical examples. This handbook is truly an indispensable guide for every professional who comes into contact with the complex material degradation and protection processes that take place under combined corrosion and wear conditions. Fields of interest include: transportation (aeronautics, maritime, rail, automotive), medical implants (orthopaedics, dentistry), biochemistry, food production, energy production, and machining. The coordination of this handbook writing was done by Professor Jean-Pierre Celis (Katholieke Universiteit Leuven, Belgium) and Professor Pierre Ponthiaux (Ecole Centrale Paris, France) assisted by twelve European experts who contributed jointly to the nine chapters of this handbook. Main topics dealt with are tribocorrosion phenomena in medical and industrial sectors, depassivation and repassivation phenomena, impact on synergism in tribocorrosion, specific testing techniques, coupling tribology-to-corrosion, design of a testing protocol, and normalisation.

Biocompatibility Protocols for Medical Devices and Materials

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Author :
Publisher : Elsevier
ISBN 13 : 0323984924
Total Pages : 264 pages
Book Rating : 4.3/5 (239 download)

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Book Synopsis Biocompatibility Protocols for Medical Devices and Materials by : Prakash Srinivasan Timiri Shanmugam

Download or read book Biocompatibility Protocols for Medical Devices and Materials written by Prakash Srinivasan Timiri Shanmugam and published by Elsevier. This book was released on 2023-04-07 with total page 264 pages. Available in PDF, EPUB and Kindle. Book excerpt: Biocompatibility Protocols for Medical Devices and Materials provides comprehensive coverage of the basic science and toxicological testing protocols necessary for the risk assessment and safety analysis of medical devices and materials which are based on the ISO guidelines for body contact and duration of contact. The book begins with device/component selection for toxicological experiments and provides an introduction to topics such as sensitization, irritation tests, material-mediated pyrogenicity, and bacterial-mediated pyrogenicity. Toxicology-related chapters explain the protocols for cytotoxicity, acute systemic toxicity, repeated-exposure systemic toxicity, genotoxicity, carcinogenicity, and reproductive toxicity testing. Biocompatibility Protocols for Medical Devices and Materials is a practical guide that provides step-by-step toxicological protocols ranging from materials selection to data interpretation for toxicologists, biomedical researchers, healthcare professionals, product developers, and others working in risk assessment and safety analysis of medical devices. - Explains the biocompatibility test protocols for medical devices - Provides an overview about chemical characterization - Describes toxicokinetic, carcinogenicity, and reproductive toxicity studies - Discusses the basic points needed to leverage the data from another device

Principles of Biomedical Sciences and Industry

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Publisher : John Wiley & Sons
ISBN 13 : 3527824006
Total Pages : 452 pages
Book Rating : 4.5/5 (278 download)

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Book Synopsis Principles of Biomedical Sciences and Industry by : Markus Hinder

Download or read book Principles of Biomedical Sciences and Industry written by Markus Hinder and published by John Wiley & Sons. This book was released on 2022-07-22 with total page 452 pages. Available in PDF, EPUB and Kindle. Book excerpt: Principles of Biomedical Sciences and Industry Improve your product development skills to bring new ideas to biomedicine The development of innovative healthcare products, such as biodegradable implants, biopharmaceuticals, or companion diagnostics, requires a multi-disciplinary approach that incorporates scientific evidence with novel and innovative ideas to create new and improved products and treatments. Indeed, product development and the integration of science with commercial aspects have become key challenges for scientists working in the pharmaceutical, biotech, and medtech industries. Using a multi-pronged approach to development, Principles of Biomedical Sciences and Industry combines ideas and methodologies from four of the central areas of focus in the biomedical arena: pharmaceuticals, diagnostics, biomaterials, and medical devices. In doing so, the book covers the entire product lifecycle, from translating a scientific idea into a prototype to product development, launch, and management. Principles of Biomedical Sciences and Industry readers will also find: Several case studies from the most important product categories (pharmaceuticals, diagnostics, medical devices, combination products) Chapters dealing with toxicology and safety risks in development, as well as regulatory approval Key business aspects including how to secure funding, managing intellectual property, and price regulation in the market An ideal resource for teachers and students that conveys the information in an easily-digestible format Ideal for advanced students and young professionals pursuing a career in the biomedical and healthcare industries, Principles of Biomedical Sciences and Industry is an essential reference for those in pharmaceutical industry, biotechnologists, medicinal chemists, bio-engineers, pharma engineers, and management consultants.

YY/T 1465.4-2017 Translated English of Chinese Standard. (YYT 1465.4-2017, YY/T1465.4-2017, YYT1465.4-2017)

Download YY/T 1465.4-2017 Translated English of Chinese Standard. (YYT 1465.4-2017, YY/T1465.4-2017, YYT1465.4-2017) PDF Online Free

Author :
Publisher : https://www.chinesestandard.net
ISBN 13 :
Total Pages : 12 pages
Book Rating : 4./5 ( download)

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Book Synopsis YY/T 1465.4-2017 Translated English of Chinese Standard. (YYT 1465.4-2017, YY/T1465.4-2017, YYT1465.4-2017) by : https://www.chinesestandard.net

Download or read book YY/T 1465.4-2017 Translated English of Chinese Standard. (YYT 1465.4-2017, YY/T1465.4-2017, YYT1465.4-2017) written by https://www.chinesestandard.net and published by https://www.chinesestandard.net. This book was released on 2018-09-01 with total page 12 pages. Available in PDF, EPUB and Kindle. Book excerpt: This Part of YY/T 1465 gives the ex-vivo method for the determination of phagocytosis of mouse peritoneal macrophages on chicken erythrocytes. This Part applies to the evaluation of the influence of medical devices/materials on phagocytic ability of macrophages.

YY/T 1465.3-2016 Translated English of Chinese Standard (YY/T 1465.3-2016, YYT1465.3-2016)

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Author :
Publisher : https://www.chinesestandard.net
ISBN 13 :
Total Pages : 12 pages
Book Rating : 4./5 ( download)

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Book Synopsis YY/T 1465.3-2016 Translated English of Chinese Standard (YY/T 1465.3-2016, YYT1465.3-2016) by : https://www.chinesestandard.net

Download or read book YY/T 1465.3-2016 Translated English of Chinese Standard (YY/T 1465.3-2016, YYT1465.3-2016) written by https://www.chinesestandard.net and published by https://www.chinesestandard.net. This book was released on 2024-03-19 with total page 12 pages. Available in PDF, EPUB and Kindle. Book excerpt: This Part of YY/T 1465 provides a method for the determination of plaque-forming cells by agar gel solid-phase method. This Part is suitable for evaluating the impact of medical devices/materials on the body's humoral immune function.

Medical Device Regulatory Practices

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Author :
Publisher : CRC Press
ISBN 13 : 9814669113
Total Pages : 578 pages
Book Rating : 4.8/5 (146 download)

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Book Synopsis Medical Device Regulatory Practices by : Val Theisz

Download or read book Medical Device Regulatory Practices written by Val Theisz and published by CRC Press. This book was released on 2015-08-03 with total page 578 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book is intended to serve as a reference for professionals in the medical device industry, particularly those seeking to learn from practical examples and case studies. Medical devices, like pharmaceuticals, are highly regulated, and the bar is raised constantly as patients and consumers expect the best-quality healthcare and safe and effectiv

Handbook of Biomaterials Biocompatibility

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Author :
Publisher : Woodhead Publishing
ISBN 13 : 0081029683
Total Pages : 759 pages
Book Rating : 4.0/5 (81 download)

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Book Synopsis Handbook of Biomaterials Biocompatibility by : Masoud Mozafari

Download or read book Handbook of Biomaterials Biocompatibility written by Masoud Mozafari and published by Woodhead Publishing. This book was released on 2020-06-17 with total page 759 pages. Available in PDF, EPUB and Kindle. Book excerpt: Handbook of Biomaterials Biocompatibility is a systematic reference on host response to different biomaterials, taking into account their physical, mechanical and chemical properties. The book reviews recent progress in the design and study of biomaterials biocompatibility, along with current understanding on how to control immune system response. Sections provide the fundamental theories and challenges of biomaterials biocompatibility, the role of different biomaterials physicochemical surface properties on cell responses, cell responses to different physicochemical properties of polymers, ceramics, metals, carbons and nanomaterials, and biomaterials in different tissues, such as the cardiac, nervous system, cartilage and bone. This resource will be suitable for those working in the fields of materials science, regenerative engineering, medicine, medical devices and nanotechnology. - Reviews the fundamental theories and challenges of biomaterials biocompatibility, including an overview of the standards and regulations - Provides an overview on the cellular and molecular mechanisms involved in host responses to biomaterials - Systematically looks at cellular response and tissue response to a wide range of biomaterials, including polymers, metals, ceramics, alloys and nanomaterials

YY/T 1465.5-2016 Translated English of Chinese Standard (YY/T 1465.5-2016, YYT1465.5-2016)

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Author :
Publisher : https://www.chinesestandard.net
ISBN 13 :
Total Pages : 17 pages
Book Rating : 4./5 ( download)

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Book Synopsis YY/T 1465.5-2016 Translated English of Chinese Standard (YY/T 1465.5-2016, YYT1465.5-2016) by : https://www.chinesestandard.net

Download or read book YY/T 1465.5-2016 Translated English of Chinese Standard (YY/T 1465.5-2016, YYT1465.5-2016) written by https://www.chinesestandard.net and published by https://www.chinesestandard.net. This book was released on 2024-04-01 with total page 17 pages. Available in PDF, EPUB and Kindle. Book excerpt: This Part of YY/T 1465 provides a method for determining the clearance rate of ¦Á-Gal antigen in medical devices of animal origin, which is suitable for the evaluation of the effectiveness of the ¦Á-Gal antigen clearance process. The method in this Part is applicable to materials that can fully expose the ¦Á-Gal antigen through grinding. If the ¦Á-Gal antigen cannot be fully exposed through grinding, other confirmed suitable methods may be considered.