Medical Device Packaging Handbook

Author : Max Sherman
Publisher : CRC Press
ISBN 13 : 0849384494
Total Pages : 414 pages
Book Rating : 4.93/5 ( download)

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Download or read book Medical Device Packaging Handbook, Revised and Expanded written by Max Sherman and published by CRC Press. This book was released on 1998-08-25 with total page 414 pages. Available in PDF, EPUB and Kindle. Book excerpt: This volume details current developments in industry practices and standards relating to medical device packaging. This edition offers entirely new as well as revised chapters on packaging materials, package validation and methods and integrity testing, bar-coding technology, environmentally sound packaging and disposal procedures, storage autoclave sytems, international standards, customer needs, regulatory aspects, and more.

Author : Joseph D. O'Brien
Publisher :
ISBN 13 :
Total Pages : 386 pages
Book Rating : 4.68/5 ( download)

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Download or read book Medical Device Packaging Handbook written by Joseph D. O'Brien and published by . This book was released on 1990 with total page 386 pages. Available in PDF, EPUB and Kindle. Book excerpt: A guide to help manufacturers, engineers, designers, and suppliers of medical products evaluate the design, materials, and technology of their packaging. Highlights recent developments in the field, and presents information on current industry standards and practices, and regulation. Provides details of materials and specifications, sterilization methods, distribution test cycles, labeling criteria, bar coding, autoclave systems, and other topics. Annotation(c) 2003 Book News, Inc., Portland, OR (booknews.com)

Author : Max Sherman
Publisher :
ISBN 13 : 9780429074691
Total Pages : pages
Book Rating : 4.97/5 ( download)

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Download or read book Medical Device Packaging Handbook, Second Edition, Revised and Expanded written by Max Sherman and published by . This book was released on 1998 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: "This volume details current developments in industry practices and standards relating to medical device packaging. This edition offers entirely new as well as revised chapters on packaging materials, package validation and methods and integrity testing, bar-coding technology, environmentally sound packaging and disposal procedures, storage autoclave sytems, international standards, customer needs, regulatory aspects, and more."--Provided by publisher.

Author : Matthew Bret Weinger
Publisher : CRC Press
ISBN 13 : 1420063510
Total Pages : 844 pages
Book Rating : 4.16/5 ( download)

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Download or read book Handbook of Human Factors in Medical Device Design written by Matthew Bret Weinger and published by CRC Press. This book was released on 2010-12-13 with total page 844 pages. Available in PDF, EPUB and Kindle. Book excerpt: Developed to promote the design of safe, effective, and usable medical devices, Handbook of Human Factors in Medical Device Design provides a single convenient source of authoritative information to support evidence-based design and evaluation of medical device user interfaces using rigorous human factors engineering principles. It offers guidance

Author : Max Sherman
Publisher : CRC Press
ISBN 13 : 9780849384493
Total Pages : 422 pages
Book Rating : 4.94/5 ( download)

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Download or read book Medical Device Packaging Handbook, Revised and Expanded written by Max Sherman and published by CRC Press. This book was released on 1998-08-25 with total page 422 pages. Available in PDF, EPUB and Kindle. Book excerpt: This volume details current developments in industry practices and standards relating to medical device packaging. This edition offers entirely new as well as revised chapters on packaging materials, package validation and methods and integrity testing, bar-coding technology, environmentally sound packaging and disposal procedures, storage autoclave sytems, international standards, customer needs, regulatory aspects, and more.

Author : Ronald Pilchik
Publisher : CRC Press
ISBN 13 : 1420014943
Total Pages : 158 pages
Book Rating : 4.45/5 ( download)

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Download or read book Validating Medical Packaging written by Ronald Pilchik and published by CRC Press. This book was released on 2002-09-27 with total page 158 pages. Available in PDF, EPUB and Kindle. Book excerpt: According to the FDA Quality System Regulations, manufacturers must ensure that "device packaging and shipping containers are designed and constructed to protect the device from alteration or damage during the customary conditions of processing, storage, handling, and distribution." As specific as this statement is, the FDA does not provide instruc

Author : Andres Diaz Lantada
Publisher : CRC Press
ISBN 13 : 9814303356
Total Pages : 546 pages
Book Rating : 4.54/5 ( download)

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Download or read book Handbook of Active Materials for Medical Devices written by Andres Diaz Lantada and published by CRC Press. This book was released on 2011-09-28 with total page 546 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book covers biodevices, mainly implantable or quirurgical, for the diagnosis or treatment of different pathologies, which benefit from the use of active materials as sensors or actuators. Such active or "intelligent" materials are capable of responding in a controlled way to different external physical or chemical stimuli by changing some of t

Author : Jack Wong
Publisher : CRC Press
ISBN 13 : 9814411213
Total Pages : 618 pages
Book Rating : 4.19/5 ( download)

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Download or read book Handbook of Medical Device Regulatory Affairs in Asia written by Jack Wong and published by CRC Press. This book was released on 2013-03-27 with total page 618 pages. Available in PDF, EPUB and Kindle. Book excerpt: Medical device regulation in Asia has gained more importance than ever. Governments and regulatory bodies across the region have put in place new regulatory systems or refined the existing ones. A registered product requires a lot of technical documentation to prove its efficacy, safety, and quality. A smooth and successful registration process demands soft skills for dealing with various key stakeholders in the government, testing centers, and hospitals and among doctors. Handbook of Medical Device Regulatory Affairs in Asia covers medical device regulatory systems in different countries, ISO standards for medical devices, clinical trial and regulatory requirements, and documentation for application. Government bodies, the medical device industry, and academics and students will find this book immensely useful in understanding the global regulatory environment and in their research and development projects.

Author : Richard C. Fries
Publisher : CRC Press
ISBN 13 : 1000693872
Total Pages : 795 pages
Book Rating : 4.74/5 ( download)

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Download or read book Handbook of Medical Device Design written by Richard C. Fries and published by CRC Press. This book was released on 2019-08-15 with total page 795 pages. Available in PDF, EPUB and Kindle. Book excerpt: First published in 2001: This handbook has been written to give those professionals working in the development and use of medical devices practical knowledge about biomedical technology, regulations, and their relationship to quality health care.

Author : Jack Wong
Publisher : CRC Press
ISBN 13 : 1000440516
Total Pages : 806 pages
Book Rating : 4.15/5 ( download)

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Download or read book Medical Regulatory Affairs written by Jack Wong and published by CRC Press. This book was released on 2022-01-27 with total page 806 pages. Available in PDF, EPUB and Kindle. Book excerpt: This handbook covers medical device regulatory systems in different countries, ISO standards for medical devices, clinical trial and regulatory requirements, and documentation for application. It is the first to cover the medical device regulatory affairs in Asia. Experts from influential international regulatory bodies, including the US Food and Drug Administration (FDA), UK Medicines and Healthcare Products Regulatory Agency, Japan Pharmaceuticals and Medical Devices Agency, Saudi Food and Drug Authority, Korea Testing Laboratory, Taiwan FDA, World Health Organization, Asian Harmonization Working Party, Regulatory Affairs Professionals Society, and British Standards Institution, have contributed to the book. Government bodies, the medical device industry, academics, students, and general readers will find the book immensely useful for understanding the global regulatory environment and in their research and development projects.