Biomedical Sciences
Technology Development and Economic Evaluation
1st Edition
Published on 15. October 2025
Book
Hardback
X, 300 pages
978-3-11-028644-1 (ISBN)
Description
This graduate-level textbook focuses on the validation and applicability of clinically relevant biomedical technologies, the market, regulatory aspects, the economic evaluation and the cost-effective pricing of medical devices. It connects the dots between devices and technologies from R&D and patient.
More details
Series
Language
English
Place of publication
Berlin/Boston
Germany
Target group
College/higher education
US School Grade: From College Freshman to College Senior
Illustrations
150 s/w Abbildungen, 100 s/w Zeichnungen, 100 s/w Tabellen
150 b/w ill., 100 b/w tbl., 100 b/w ld
Dimensions
Height: 24 cm
Width: 17 cm
ISBN-13
978-3-11-028644-1 (9783110286441)
Schweitzer Classification
Persons
Bob Gauvin and Maxime D. Guillemette, Université Laval, Québec, Canada.
Content
From the Contents
Validation and applicability of clinically relevant biomedical technologies
Fields of application for biomedical technologies
- Medical devices market
- Diagnostic devices market
- Cosmetic products market
- Medical devices in emerging markets
Regulatory aspects: Protecting the public and the patient
- Protecting your idea with intellectual property
- FDA regulatory processes
- Regulatory processes to obtain CE marking
Bringing biomedical devices and technologies from R&D to the patient
- Fundraising and sound management of the assets
- Manufacturing of tissue engineered products
- Manufacturing and scaling up biological products
- Manufacturing and engineering of medical devices
- Clinical trials
- Entering the market with innovative biomedical technologies
Economic evaluation of innovative medical devices
- Basic principles for economic evaluation
- Cost-effectiveness and pricing of medical devices
Validation and applicability of clinically relevant biomedical technologies
Fields of application for biomedical technologies
- Medical devices market
- Diagnostic devices market
- Cosmetic products market
- Medical devices in emerging markets
Regulatory aspects: Protecting the public and the patient
- Protecting your idea with intellectual property
- FDA regulatory processes
- Regulatory processes to obtain CE marking
Bringing biomedical devices and technologies from R&D to the patient
- Fundraising and sound management of the assets
- Manufacturing of tissue engineered products
- Manufacturing and scaling up biological products
- Manufacturing and engineering of medical devices
- Clinical trials
- Entering the market with innovative biomedical technologies
Economic evaluation of innovative medical devices
- Basic principles for economic evaluation
- Cost-effectiveness and pricing of medical devices