Medical Device Design: Innovation from concept to market (Hardcover)
暫譯: 醫療器材設計:從概念到市場的創新 (精裝版)
Peter J Ogrodnik
- 出版商: Academic Press
- 出版日期: 2012-12-04
- 售價: $5,390
- 貴賓價: 9.5 折 $5,121
- 語言: 英文
- 頁數: 376
- 裝訂: Hardcover
- ISBN: 0123919428
- ISBN-13: 9780123919427
海外代購書籍(需單獨結帳)
買這商品的人也買了...
-
$720$562 -
$520$411 -
$490$387 -
$520$411 -
$650$514 -
$680$537 -
$580$458 -
$650$553 -
$400$340 -
$540$459 -
$1,000$700 -
$280$238 -
$680$537 -
$650$514 -
$750$638 -
$580$452 -
$1,130$893 -
$480$379 -
$880$686 -
$450$356 -
$520$442 -
$380$199 -
$480$408 -
$680$578 -
$280$238
商品描述
This book provides the bridge between engineering design and medical devices 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 authors' years of experience in academia (R&D phase) and industrial (commercialization phase) experience. This design methodology enables engineers and medical device manufacturers to bring new products to the market place 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.
商品描述(中文翻譯)
這本書提供了工程設計與醫療設備開發之間的橋樑。沒有單一的文本能夠涵蓋醫療設備設計師在開發新產品或改進舊產品時所面臨的眾多設計問題。它探討了醫療設備的法規(FDA 和 EU)要求:這些是全球最嚴格的工程要求之一。未能滿足這些要求的工程師可能會對使用者造成嚴重傷害,並影響其產品的商業前景。本手冊展示了醫療設計師必須理解的基本方法論,以確保其產品符合要求。它整合了經過驗證的設計協議,並將其置於明確的醫療背景中,基於作者在學術界(研發階段)和工業界(商業化階段)的多年經驗。這種設計方法論使工程師和醫療設備製造商能夠迅速將新產品推向市場。
- 醫療設備市場是一個數十億美元的產業。這個領域的每一個工程產品,從手術刀到支架,再到複雜的醫療設備,都必須按照批准的程序和標準進行設計和開發。本書展示了如何做到這一點。
- 涵蓋美國、歐盟和 ISO 標準,實現真正的國際化方法,提供實踐工程師所需理解的國際標準指南。
- 由經驗豐富的醫療設備工程師和企業家撰寫,他們在美國和英國擁有產品,並具備開發和商業化醫療產品的實際經驗。