Richard C. Fries – författare

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16 produkter

Handbook of Medical Device Design
AvRichard C. Fries
Inbunden, Engelska, 2019
3 797 kr
Skickas inom 10-15 vardagar
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.
Handbook of Medical Device Design
AvRichard C. Fries
Häftad, Engelska, 2021
1 100 kr
Skickas inom 10-15 vardagar
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.
Medical Device Quality Assurance and Regulatory Compliance
AvRichard C. Fries
Häftad, Engelska, 2019
957 kr
Skickas inom 10-15 vardagar
"Acquaints developers of medical devices with the basic concepts and major issues of medical quality assurance and regulatory documents, describes the requirements listed in these documents, and provides strategies for compliance with these requirements."
Design of Biomedical Devices and Systems, 4th edition
AvArthur T. Johnson,Richard C. Friesm. fl.
E-bok
Engelska, 2018
2 849 kr
Läs direkt efter köp
This fourth edition is a substantial revision of a highly regarded text, intended for senior design capstone courses within departments of biomedical engineering, bioengineering, biological engineering and medical engineering, worldwide. Each chapter has been thoroughly updated and revised to reflect the latest developments. New material has been added on entrepreneurship, bioengineering design, clinical trials and CRISPR. Based upon feedback from prior users and reviews, additional and new examples and applications, such as 3D printing have been added to the text. Additional clinical applications were added to enhance the overall relevance of the material presented. Relevant FDA regulations and how they impact the designer’s work have been updated.
Features

Provides updated material as needed to each chapter

Incorporates new examples and applications within each chapter

Discusses new material related to entrepreneurship, clinical trials and CRISPR

Relates critical new information pertaining to FDA regulations.

Presents new material on "discovery" of projects "worth pursuing" and design for health care for low-resource environments

Presents multiple case examples of entrepreneurship in this field

Addresses multiple safety and ethical concerns for the design of medical devices and processes
Design of Biomedical Devices and Systems, 4th edition
AvArthur T. Johnson,Richard C. Friesm. fl.
E-bok
PDF, Engelska, 2018
2 879 kr
Läs direkt efter köp
This fourth edition is a substantial revision of a highly regarded text, intended for senior design capstone courses within departments of biomedical engineering, bioengineering, biological engineering and medical engineering, worldwide. Each chapter has been thoroughly updated and revised to reflect the latest developments. New material has been added on entrepreneurship, bioengineering design, clinical trials and CRISPR. Based upon feedback from prior users and reviews, additional and new examples and applications, such as 3D printing have been added to the text. Additional clinical applications were added to enhance the overall relevance of the material presented. Relevant FDA regulations and how they impact the designer’s work have been updated.
Features

Provides updated material as needed to each chapter

Incorporates new examples and applications within each chapter

Discusses new material related to entrepreneurship, clinical trials and CRISPR

Relates critical new information pertaining to FDA regulations.

Presents new material on "discovery" of projects "worth pursuing" and design for health care for low-resource environments

Presents multiple case examples of entrepreneurship in this field

Addresses multiple safety and ethical concerns for the design of medical devices and processes
Medical Device Quality Assurance and Regulatory Compliance
AvRichard C. Fries
Inbunden, Engelska, 1998
7 587 kr
Skickas inom 10-15 vardagar
"Acquaints developers of medical devices with the basic concepts and major issues of medical quality assurance and regulatory documents, describes the requirements listed in these documents, and provides strategies for compliance with these requirements."
Handbook of Medical Device Design
AvRichard C. Fries
E-bok
PDF, Engelska, 2019
1 157 kr
Läs direkt efter köp
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.
Handbook of Medical Device Design
AvRichard C. Fries
E-bok
Engelska, 2019
1 299 kr
Läs direkt efter köp
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.
Reliable Design of Medical Devices
AvRichard C. Fries
E-bok
Engelska, 2016
1 899 kr
Läs direkt efter köp
As medical devices become even more intricate, concerns about efficacy, safety, and reliability continue to be raised. Users and patients both want the device to operate as specified, perform in a safe manner, and continue to perform over a long period of time without failure. Following in the footsteps of the bestselling second edition, Reliable D
Medical Device Quality Assurance and Regulatory Compliance
AvRichard C. Fries
E-bok
Engelska, 1998
1 126 kr
Läs direkt efter köp
"Acquaints developers of medical devices with the basic concepts and major issues of medical quality assurance and regulatory documents, describes the requirements listed in these documents, and provides strategies for compliance with these requirements."
Reliable Design of Medical Devices
AvRichard C. Fries
Häftad, Engelska, 2017
1 610 kr
Skickas inom 10-15 vardagar
As medical devices become even more intricate, concerns about efficacy, safety, and reliability continue to be raised. Users and patients both want the device to operate as specified, perform in a safe manner, and continue to perform over a long period of time without failure. Following in the footsteps of the bestselling second edition, Reliable Design of Medical Devices, Third Edition shows you how to improve reliability in the design of advanced medical devices. Reliability engineering is an integral part of the product development process and of problem-solving activities related to manufacturing and field failures. Mirroring the typical product development process, the book is organized into seven parts. After an introduction to the basics of reliability engineering and failures, it takes you through the concept, feasibility, design, verification and validation, design transfer and manufacturing, and field activity phases. Topics covered include Six Sigma for design, human factors, safety and risk analysis, and new techniques such as accelerated life testing (ALT) and highly accelerated life testing (HALT).What’s New in This EditionUpdates throughout, reflecting changes in the fieldAn updated software development processUpdated hardware test proceduresA new layout that follows the product development processA list of deliverables needed at the end of each development phaseIncorporating reliability engineering as a fundamental design philosophy, this book shares valuable insight from the author’s more than 35 years of experience. A practical guide, it helps you develop a more effective reliability engineering program—contributing to increased profitability, more satisfied customers, and less risk of liability.
Design of Biomedical Devices and Systems, 4th edition
AvPaul H. King,Richard C. Friesm. fl.
Inbunden, Engelska, 2018
2 412 kr
Skickas inom 10-15 vardagar
This fourth edition is a substantial revision of a highly regarded text, intended for senior design capstone courses within departments of biomedical engineering, bioengineering, biological engineering and medical engineering, worldwide. Each chapter has been thoroughly updated and revised to reflect the latest developments. New material has been added on entrepreneurship, bioengineering design, clinical trials and CRISPR. Based upon feedback from prior users and reviews, additional and new examples and applications, such as 3D printing have been added to the text. Additional clinical applications were added to enhance the overall relevance of the material presented. Relevant FDA regulations and how they impact the designer’s work have been updated.Features Provides updated material as needed to each chapter Incorporates new examples and applications within each chapter Discusses new material related to entrepreneurship, clinical trials and CRISPR Relates critical new information pertaining to FDA regulations. Presents new material on "discovery" of projects "worth pursuing" and design for health care for low-resource environments Presents multiple case examples of entrepreneurship in this field Addresses multiple safety and ethical concerns for the design of medical devices and processes
Reliable Design of Medical Devices
AvRichard C. Fries
Inbunden, Engelska, 2012
4 234 kr
Skickas inom 10-15 vardagar
As medical devices become even more intricate, concerns about efficacy, safety, and reliability continue to be raised. Users and patients both want the device to operate as specified, perform in a safe manner, and continue to perform over a long period of time without failure. Following in the footsteps of the bestselling second edition, Reliable Design of Medical Devices, Third Edition shows you how to improve reliability in the design of advanced medical devices. Reliability engineering is an integral part of the product development process and of problem-solving activities related to manufacturing and field failures. Mirroring the typical product development process, the book is organized into seven parts. After an introduction to the basics of reliability engineering and failures, it takes you through the concept, feasibility, design, verification and validation, design transfer and manufacturing, and field activity phases. Topics covered include Six Sigma for design, human factors, safety and risk analysis, and new techniques such as accelerated life testing (ALT) and highly accelerated life testing (HALT).What’s New in This EditionUpdates throughout, reflecting changes in the fieldAn updated software development processUpdated hardware test proceduresA new layout that follows the product development processA list of deliverables needed at the end of each development phaseIncorporating reliability engineering as a fundamental design philosophy, this book shares valuable insight from the author’s more than 35 years of experience. A practical guide, it helps you develop a more effective reliability engineering program—contributing to increased profitability, more satisfied customers, and less risk of liability.
Reliable Design of Medical Devices
AvRichard C. Fries
E-bok
PDF, Engelska, 2016
1 818 kr
Läs direkt efter köp
As medical devices become even more intricate, concerns about efficacy, safety, and reliability continue to be raised. Users and patients both want the device to operate as specified, perform in a safe manner, and continue to perform over a long period of time without failure. Following in the footsteps of the bestselling second edition, Reliable D
Medical Device Quality Assurance and Regulatory Compliance
AvRichard C. Fries
E-bok
PDF, Engelska, 1998
1 138 kr
Läs direkt efter köp
"Acquaints developers of medical devices with the basic concepts and major issues of medical quality assurance and regulatory documents, describes the requirements listed in these documents, and provides strategies for compliance with these requirements."
Handbook of Medical Device Design
AvRichard C. Fries
Inbunden, Engelska, 2000
4 018 kr
Tillfälligt slut
The Handbook of Medical Device Design provides a review of regulatory and standards issues in medical device design, including FDA regulations, types of 510 (k), the ISO 9000 series, and medical device directives. It identifies how to determine and document customer needs and device requirements. It also establishes reliability and quality metrics for the duration of the product development cycle. Topics include

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Richard C. Fries – författare

Handbook of Medical Device Design

Handbook of Medical Device Design

Medical Device Quality Assurance and Regulatory Compliance

Design of Biomedical Devices and Systems, 4th edition

Design of Biomedical Devices and Systems, 4th edition

Medical Device Quality Assurance and Regulatory Compliance

Handbook of Medical Device Design

Handbook of Medical Device Design

Reliable Design of Medical Devices

Medical Device Quality Assurance and Regulatory Compliance

Reliable Design of Medical Devices

Design of Biomedical Devices and Systems, 4th edition

Reliable Design of Medical Devices

Reliable Design of Medical Devices

Medical Device Quality Assurance and Regulatory Compliance

Handbook of Medical Device Design

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