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Medical Devices: Regulations, Standards and PracticesBy Seeram Ramakrishna, Lingling Tian, Charlene Wang, Susan Liao, Wee Eong Teo
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Medical Devices and Regulations: Standards and Practices will shed light on the importance of regulations and standards among all stakeholders, bioengineering designers, biomaterial scientists and researchers to enable development of future medical devices.
Based on the authors’ practical experience, this book provides a concise, practical guide on key issues and processes in developing new medical devices to meet international regulatory requirements and standards.
- Provides readers with a global perspective on medical device regulations
- Concise and comprehensive information on how to design medical devices to ensure they meet regulations and standards
- Includes a useful case study demonstrating the design and approval process
- Sales Rank: #983025 in Books
- Published on: 2015-12-24
- Original language: English
- Number of items: 1
- Dimensions: 9.10" h x .70" w x 6.00" l, 1.25 pounds
- Binding: Hardcover
- 256 pages
From the Back Cover
Based on the authors’ practical experience, this book provides a concise, practical guide on key issues and processes in developing new medical devices to meet international regulatory requirements and standards.
Medical Devices and Regulations: Standards and Practices will shed light on the importance of regulations and standards among all stakeholders, bioengineering designers, biomaterial scientists and researchers to enable development of future medical devices.
Part One, covers the worldwide regulation of medical devices, management systems, standards for medical device manufacture, and the process of gaining approval for new medical devices. In addition, including recent changes to the regulations and standards.
In Part Two, we provide guidance on risk assessment procedures for new medical devices and safety and clinical testing based on 3 main ISO standards. Based on the latest version of those standards, we illustrate current standards and guidance documents.
In Part Three, we discuss the practices: product design overview, case studies and highlight the role of the international medical device regulator forum in the pursuit of global harmonization.
Professor Dr PE Seeram Ramakrishna, FREng, is the Director of Center for Nanofibers & Nanotechnology at the National University of Singapore and an Elected fellow Royal Academy of Engineering, UK; Institution of Engineers Singapore; and American Institute for Medical & Biological Engineering. Dr. Tian Lingling is a Research Fellow at National University of Singapore, Singapore. Ms. Charlene Wang has five years’ experience in biomedical research laboratory management. Dr. Susan Liao is Programme manager and Senior Research Fellow at Nanyang Technological University, Singapore. Mr Teo Wee Eong has over a decade of academic and industrial experience in medical devices ranging from single component implantable to electrical medical device. He is currently a senior product engineer responsible for ensuring compliance of medical devices.
About the Author
Prof Seeram Ramakrishna is the Director of the Center for Nanofibers & Nanotechnology at the National University of Singapore. He has received awards and recognitions for his pioneering contributions to the field of biomaterials. He specialises in design, processing and validation of biomimetic scaffolds for regeneration of various tissues. He pioneered translucent biomaterials and devices, which are now manufactured and marketed globally by Biomers International. He is an elected international fellow of the Royal Academy of Engineering, UK; Institution of Engineers Singapore; and the American Institute for Medical & Biological Engineering. His research has been translated into products which are available in several countries. He has authored 6 books and more than 500 journal papers.
Dr. Tian Lingling is a Research Fellow at National University of Singapore, Singapore. She obtained her Ph.D in Textile Engineering from College of Textiles, Donghua University, Shanghai, China in March of 2014. Her research interests include fabrication of electrospun nanofibers and electrosprayed nano/micro-particles, and the application in cardiac, bone and nerve tissue engineering. She has around 10 peer-reviewed journal/conference paper/book chapter publications and one patent.
Dr. Susan Liao is Programme manager and Senior Research Fellow at Nanyang Technological University, Singapore. She was Lee Kuan Yew Research Fellow in the Division of Bioengineering and Department of Orthopaedic Surgery, National University of Singapore. She obtained her Ph.D in Biomaterials from the Department of Materials Science and Engineering, Tsinghua University, Beijing, China. Her research interests include Tissue Engineering, Biomimetic nanomaterials, Biomineralization and Cell-biomimetic matrix reactions. She has around 80 peer-reviewed journal/book chapter publications and over 40 international conference presentations. She has also served as an editorial board member for four professional journals and as a reviewer for over forty professional journals.
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