Review

Using an engineering approach, the fundamentals of electronic medical devices are presented along with the basic medical knowledge deemed necessary for design considerations. After addressing power subsystems, chapters address a range of sensors. The processes of data acquisition and digital signal processing are also considered. The material is accompanied by examples of technologies and numerous schematic diagrams.Book News, Inc.r, Portland, OR — Review

Review

Using an engineering approach, the fundamentals of electronic medical devices are presented along with the basic medical knowledge deemed necessary for design considerations. After addressing power subsystems, chapters address a range of sensors. The processes of data acquisition and digital signal processing are also considered. The material is accompanied by examples of technologies and numerous schematic diagrams.Book News, Inc.®, Portland, OR

See all Editorial Rev (more…)

Future generations of vital signs and point-of-care medical devices must interoperate directly and seamlessly with information technology systems to facilitate effective patient care management within the healthcare enterprise. This is the first book addressing medical device integration with the computer-based patient record in a holistic way. Readers step into the area of two-way device communication & control and learn best practises from an author known for his brilliant expertise in this field. It is a fundamental guide for a broad group of people: clinical and biomedical engineers, physicians, bioinformatics practitioners, and vendors. Providing the essential how-to for medical device integration into the electronic medical record (EMR), health information system (HIS), and computerized patient record (CPR), the book highlights information on data extraction, usually not offered by device vendors. This comprises topics such as the use of third-party software, (more…)

An essential introduction to conducting the various stages of medical device clinical trials Clinical research continues to be one of the most vital components of pharmaceutical, biostatistical, and medical studies. Design, Execution, and Management of Medical Device Clinical Trials provides a uniform methodology for conducting and managing clinical trials. Written in a style that is accessible to readers from diverse educational and professional backgrounds, this book provides an in-depth and broad overview for successfully performing clinical tasks and activities. Throughout the book, practical examples compiled from both the author’s and other researchers’ previous clinical trial experiences are discussed in a sequential manner as they occur in the study, starting from the development of the clinical protocol and the selection of clinical sites and ending with the completion of the final clinical study report. Next, readers are guided through the devel (more…)

Review

Using an engineering approach, the fundamentals of electronic medical devices are presented along with the basic medical knowledge deemed necessary for design considerations. After addressing power subsystems, chapters address a range of sensors. The processes of data acquisition and digital signal processing are also considered. The material is accompanied by examples of technologies and numerous schematic diagrams.Book News, Inc.r, Portland, OR — Review

Review

Using an engineering approach, the fundamentals of electronic medical devices are presented along with the basic medical knowledge deemed necessary for design considerations. After addressing power subsystems, chapters address a range of sensors. The processes of data acquisition and digital signal processing are also considered. The material is accompanied by examples of technologies and numerous schematic diagrams.Book News, Inc.®, Portland, OR

See all Editorial Rev (more…)

Review

“This book is an absolute must for anybody who is just overwhelmed by the prospect of having to go through the various standards that are becoming increasingly important to manufacturers and users alike. . ..It not only explains every aspect of the science of reliable design but provides clear definitions of the jargon and good practical examples of the paperwork required from the various certifying bodies. . . .it is unlikely that most of us will ever need to refer to any other book than this one. ” —Proceedings of the Institution of Mechanical Engineers
–This text refers to an out of print or unavailable edition of this title.

As medical devices increase in complexity, concerns about efficacy, safety, quality, and longevity increase in stride. Introduced nearly a decade ago, Reliable Design of Medical Devices illuminated the path to increased reliability in the hands-on design of advanced medical devices. With fully updated coverage in its (more…)

This reference provides real-world examples, strategies, and templates for the implementation of effective design control programs that meet current ISO 9000 and FDA QSR standards and regulations-offering product development models for the production of safe, durable, and cost-efficient medical devices and systems.Details procedures utilized by leading companies to successfully meet FDA and end-user requirements, manufacture high-quality products, and improve and generate profit.Design Controls for the Medical Device Industry contains valuable guidelines that enable readers to prepare for an FDA audit identify consumer needs, resolve project objectives, and process inconsistencies and discrepancies determine the compatibility of design specifications and manufacturing, installation, and servicing demands ensure that proper design, function, and performance stipulations are understood and met verify and validate design criteria and production schemes eliminate confusion an (more…)

Review
“This book is an absolute must for anybody who is just overwhelmed by the prospect of having to go through the various standards that are becoming increasingly important to manufacturers and users alike. . ..It not only explains every aspect of the science of reliable design but provides clear definitions of the jargon and good practical examples of the paperwork required from the various certifying bodies. . . .it is unlikely that most of us will ever need to refer to any other book than this one. ” —Proceedings of the Institution of Mechanical Engineers

As medical devices increase in complexity, concerns about efficacy, safety, quality, and longevity increase in stride. Introduced nearly a decade ago, Reliable Design of Medical Devices illuminated the path to increased reliability in the hands-on design of advanced medical devices. With fully updated coverage in its Second Edition, this practical guide continues to be the benchmark for incorporating relia (more…)

Future generations of vital signs and point-of-care medical devices must interoperate directly and seamlessly with information technology systems to facilitate effective patient care management within the healthcare enterprise. This is the first book addressing medical device integration with the computer-based patient record in a holistic way. Readers step into the area of two-way device communication & control and learn best practises from an author known for his brilliant expertise in this field. It is a fundamental guide for a broad group of people: clinical and biomedical engineers, physicians, bioinformatics practitioners, and vendors. Providing the essential how-to for medical device integration into the electronic medical record (EMR), health information system (HIS), and computerized patient record (CPR), the book highlights information on data extraction, usually not offered by device vendors. This comprises topics such as the use of third-party software, inf (more…)