Medical Device Design: Innovation from concept to market

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9780123919427: Medical Device Design: Innovation from concept to market

This book provides the bridge between engineering design and medical device development. There is no single text that addresses the plethora of design issues a medical devices designer meets when developing new products or improving older ones. It addresses medical devices' regulatory (FDA and EU) requirements--some of the most stringent engineering requirements globally. Engineers failing to meet these requirements can cause serious harm to users as well as their products' commercial prospects. This Handbook shows the essential methodologies medical designers must understand to ensure their products meet requirements. It brings together proven design protocols and puts them in an explicit medical context based on the author's years of academia (R&D phase) and industrial (commercialization phase) experience. This design methodology enables engineers and medical device manufacturers to bring new products to the marketplace rapidly.



      • The medical device market is a multi-billion dollar industry. Every engineered product for this sector, from scalpelsstents to complex medical equipment, must be designed and developed to approved procedures and standards. This book shows how.
      • Covers US, and EU and ISO standards, enabling a truly international approach, providing a guide to the international standards that practicing engineers require to understand.
      • Written by an experienced medical device engineers and entrepreneurs with products in the from the US and UK and with real world experience of developing and commercializing medical products.

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      Ogrodnik, Peter J
      ISBN 10: 0123919428 ISBN 13: 9780123919427
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      Ogrodnik, Peter J
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      Book Description Academic Press, 2012. Book Condition: New. Brand New, Unread Copy in Perfect Condition. A+ Customer Service! Summary: Design, develop and bring medical devices to market successfully by following this integrated approach to designing recognized US and EU procedures. Bookseller Inventory # ABE_book_new_0123919428

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      Book Description Elsevier Science Publishing Co Inc, United States, 2012. Hardback. Book Condition: New. New.. 236 x 194 mm. Language: English . Brand New Book. This book provides the bridge between engineering design and medical device development. There is no single text that addresses the plethora of design issues a medical devices designer meets when developing new products or improving older ones. It addresses medical devices regulatory (FDA and EU) requirements--some of the most stringent engineering requirements globally. Engineers failing to meet these requirements can cause serious harm to users as well as their products commercial prospects. This Handbook shows the essential methodologies medical designers must understand to ensure their products meet requirements. It brings together proven design protocols and puts them in an explicit medical context based on the author s years of academia (RD phase) and industrial (commercialization phase) experience. This design methodology enables engineers and medical device manufacturers to bring new products to the marketplace rapidly. Bookseller Inventory # AA59780123919427

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      Book Description Elsevier Science Publishing Co Inc, United States, 2012. Hardback. Book Condition: New. New.. 236 x 194 mm. Language: English . Brand New Book. This book provides the bridge between engineering design and medical device development. There is no single text that addresses the plethora of design issues a medical devices designer meets when developing new products or improving older ones. It addresses medical devices regulatory (FDA and EU) requirements--some of the most stringent engineering requirements globally. Engineers failing to meet these requirements can cause serious harm to users as well as their products commercial prospects. This Handbook shows the essential methodologies medical designers must understand to ensure their products meet requirements. It brings together proven design protocols and puts them in an explicit medical context based on the author s years of academia (RD phase) and industrial (commercialization phase) experience. This design methodology enables engineers and medical device manufacturers to bring new products to the marketplace rapidly. Bookseller Inventory # AA59780123919427

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      Book Description Book Condition: New. Publisher/Verlag: Academic Press | Innovation from concept to market | This book provides the bridge between engineering design and medical device development. There is no single text that addresses the plethora of design issues a medical devices designer meets when developing new products or improving older ones. It addresses medical devices' regulatory (FDA and EU) requirements--some of the most stringent engineering requirements globally. Engineers failing to meet these requirements can cause serious harm to users as well as their products' commercial prospects. This Handbook shows the essential methodologies medical designers must understand to ensure their products meet requirements. It brings together proven design protocols and puts them in an explicit medical context based on the author's years of academia (R&D phase) and industrial (commercialization phase) experience. This design methodology enables engineers and medical device manufacturers to bring new products to the marketplace rapidly.The medical device market is a multi-billion dollar industry. Every engineered product for this sector, from scalpelsstents to complex medical equipment, must be designed and developed to approved procedures and standards. This book shows howCovers US, and EU and ISO standards, enabling a truly international approach, providing a guide to the international standards that practicing engineers require to understandWritten by an experienced medical device engineers and entrepreneurs with products in the from the US and UK and with real world experience of developing and commercializing medical products | IntroductionClassifying medical devicesThe design process Implementing design proceduresDeveloping your product design specificationGenerating ideas and concepts Quality in designDesign realization/Detailed designEvaluation (validation and verification)Manufacturing supply chain Labeling and instructions for usePostmarket surveilanceProtecting your IPObtaining regulatory approval to market | Format: Hardback | Language/Sprache: english | 832 gr | 245x196x29 mm | 376 pp. Bookseller Inventory # K9780123919427

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